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<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Front cover</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob90082j</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>197</fpage>
<lpage>198</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob90082j">Abstract</self-uri>
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<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Contents list</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob90083h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>199</fpage>
<lpage>210</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob90083h">Abstract</self-uri>
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<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A one-pot catalysis: the strategic classification with some recent examples</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06432k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Patil</surname>
<given-names>Nitin T.</given-names></name>
<name><surname>Shinde</surname>
<given-names>Valmik S.</given-names></name>
<name><surname>Gajula</surname>
<given-names>Balakrishna</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>211</fpage>
<lpage>224</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06432k">Abstract</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Iron-catalyzed ene-type propargylation of diarylethylenes with propargyl alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06456h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Peng</surname>
<given-names>Shiyong</given-names></name>
<name><surname>Wang</surname>
<given-names>Lei</given-names></name>
<name><surname>Wang</surname>
<given-names>Jian</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>225</fpage>
<lpage>228</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06456h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06456h">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06456h">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quick and highly efficient copper-catalyzed cycloaddition of organic azides with terminal alkynes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06190a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wang</surname>
<given-names>Dong</given-names></name>
<name><surname>Zhao</surname>
<given-names>Mingming</given-names></name>
<name><surname>Liu</surname>
<given-names>Xiang</given-names></name>
<name><surname>Chen</surname>
<given-names>Yongxin</given-names></name>
<name><surname>Li</surname>
<given-names>Na</given-names></name>
<name><surname>Chen</surname>
<given-names>Baohua</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>229</fpage>
<lpage>231</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06190a">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photoinduced chlorine atom-transfer cyclization/photohydrolysis of 3-acyl-2-chloro-&lt;i&gt;N&lt;/i&gt;-(ω-phenylalkynyl)pyrroles: a one-pot synthesis of benzoyl-substituted fused pyrroles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob05954h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lu</surname>
<given-names>Shen-Ci</given-names></name>
<name><surname>Wang</surname>
<given-names>Wei-Xia</given-names></name>
<name><surname>Gao</surname>
<given-names>Pan-Liang</given-names></name>
<name><surname>Zhang</surname>
<given-names>Wei</given-names></name>
<name><surname>Tu</surname>
<given-names>Zhi-Feng</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>232</fpage>
<lpage>235</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob05954h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob05954h">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob05954h">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Asymmetric hydroxyamination of oxindoles catalyzed by chiral bifunctional tertiary amine thiourea: construction of 3-amino-2-oxindoles with quaternary stereocenters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06413d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jia</surname>
<given-names>Li-Na</given-names></name>
<name><surname>Huang</surname>
<given-names>Jun</given-names></name>
<name><surname>Peng</surname>
<given-names>Lin</given-names></name>
<name><surname>Wang</surname>
<given-names>Liang-Liang</given-names></name>
<name><surname>Bai</surname>
<given-names>Jian-Fei</given-names></name>
<name><surname>Tian</surname>
<given-names>Fang</given-names></name>
<name><surname>He</surname>
<given-names>Guang-Yun</given-names></name>
<name><surname>Xu</surname>
<given-names>Xiao-Ying</given-names></name>
<name><surname>Wang</surname>
<given-names>Li-Xin</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>236</fpage>
<lpage>239</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06413d">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06413d">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06413d">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ruthenium-catalysed oxidative synthesis of heterocycles from alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06516e</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Watson</surname>
<given-names>Andrew J. A.</given-names></name>
<name><surname>Maxwell</surname>
<given-names>Aoife C.</given-names></name>
<name><surname>Williams</surname>
<given-names>Jonathan M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>240</fpage>
<lpage>243</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06516e">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06516e">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06516e">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of functionalized 2,3-dihydroisoxazoles by domino reactions in water and unexpected ring-opening reactions of 2,3-dihydroisoxazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06318a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Li</surname>
<given-names>Ping</given-names></name>
<name><surname>Teng</surname>
<given-names>Bo-Tao</given-names></name>
<name><surname>Jin</surname>
<given-names>Fa-Gen</given-names></name>
<name><surname>Li</surname>
<given-names>Xin-Sheng</given-names></name>
<name><surname>Zhu</surname>
<given-names>Wei-Dong</given-names></name>
<name><surname>Xie</surname>
<given-names>Jian-Wu</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>244</fpage>
<lpage>247</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06318a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06318a">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06318a">PDF</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Microwave-assisted benzyl-transfer reactions of commercially available 2-benzyloxy-1-methylpyridinium triflate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06504a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wang</surname>
<given-names>Teng-wei</given-names></name>
<name><surname>Intaranukulkit</surname>
<given-names>Tanit</given-names></name>
<name><surname>Rosana</surname>
<given-names>Michael R.</given-names></name>
<name><surname>Slegeris</surname>
<given-names>Rimantas</given-names></name>
<name><surname>Simon</surname>
<given-names>Janet</given-names></name>
<name><surname>Dudley</surname>
<given-names>Gregory B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>248</fpage>
<lpage>250</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06504a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06504a">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06504a">PDF</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Design, synthesis, and application of tartaric acid derived &lt;i&gt;N&lt;/i&gt;-spiro quaternary ammonium salts as chiral phase-transfer catalysts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06573d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Waser</surname>
<given-names>Mario</given-names></name>
<name><surname>Gratzer</surname>
<given-names>Katharina</given-names></name>
<name><surname>Herchl</surname>
<given-names>Richard</given-names></name>
<name><surname>Müller</surname>
<given-names>Norbert</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>251</fpage>
<lpage>254</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06573d">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06573d">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06573d">PDF</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Self-association-driven transition of the β-peptidic H12 helix to the H18 helix</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06627g</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Szolnoki</surname>
<given-names>Éva</given-names></name>
<name><surname>Hetényi</surname>
<given-names>Anasztázia</given-names></name>
<name><surname>Martinek</surname>
<given-names>Tamás A.</given-names></name>
<name><surname>Szakonyi</surname>
<given-names>Zsolt</given-names></name>
<name><surname>Fülöp</surname>
<given-names>Ferenc</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>255</fpage>
<lpage>259</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06627g">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06627g">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06627g">PDF</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Flexible oligocholate foldamers as membrane transporters and their guest-dependent transport mechanism</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06364b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Zhang</surname>
<given-names>Shiyong</given-names></name>
<name><surname>Zhao</surname>
<given-names>Yan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>260</fpage>
<lpage>266</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06364b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06364b">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06364b">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>6-Hydroxyindole-based borondipyrromethene: Synthesis and spectroscopic studies</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06200j</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Zhao</surname>
<given-names>Chunchang</given-names></name>
<name><surname>Feng</surname>
<given-names>Peng</given-names></name>
<name><surname>Cao</surname>
<given-names>Jian</given-names></name>
<name><surname>Zhang</surname>
<given-names>Yulin</given-names></name>
<name><surname>Wang</surname>
<given-names>Xuzhe</given-names></name>
<name><surname>Yang</surname>
<given-names></given-names></name>
<name><surname>Zhang</surname>
<given-names>Yanfen</given-names></name>
<name><surname>Zhang</surname>
<given-names>Jinxin</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>267</fpage>
<lpage>272</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06200j">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06200j">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06200j">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Site-specific protein double labeling by expressed protein ligation: applications to repeat proteins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06397a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rosa</surname>
<given-names>Lucia De</given-names></name>
<name><surname>Cortajarena</surname>
<given-names>Aitziber L.</given-names></name>
<name><surname>Romanelli</surname>
<given-names>Alessandra</given-names></name>
<name><surname>Regan</surname>
<given-names>Lynne</given-names></name>
<name><surname>D'Andrea</surname>
<given-names>Luca Domenico</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>273</fpage>
<lpage>280</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06397a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06397a">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06397a">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Lack of correlation between catalytic efficiency and basicity of amines during the reaction of aryl methyl ketones with DMF-DMA: an unprecedented supramolecular domino catalysis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06043k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sarkar</surname>
<given-names>Anirban</given-names></name>
<name><surname>Roy</surname>
<given-names>Sudipta Raha</given-names></name>
<name><surname>Kumar</surname>
<given-names>Dinesh</given-names></name>
<name><surname>Madaan</surname>
<given-names>Chetna</given-names></name>
<name><surname>Rudrawar</surname>
<given-names>Santosh</given-names></name>
<name><surname>Chakraborti</surname>
<given-names>Asit K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>281</fpage>
<lpage>286</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06043k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06043k">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06043k">PDF</self-uri>
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</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>ParaCEST MRI contrast agents capable of derivatization &lt;i&gt;via&lt;/i&gt;“click” chemistry</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06162c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Milne</surname>
<given-names>Mark</given-names></name>
<name><surname>Chicas</surname>
<given-names>Kirby</given-names></name>
<name><surname>Li</surname>
<given-names>Alex</given-names></name>
<name><surname>Bartha</surname>
<given-names>Robert</given-names></name>
<name><surname>Hudson</surname>
<given-names>Robert H. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>287</fpage>
<lpage>292</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06162c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06162c">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06162c">PDF</self-uri>
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</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Selective &lt;i&gt;N&lt;/i&gt;-alkylation of amines using nitriles under hydrogenation conditions: facile synthesis of secondary and tertiary amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06303k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ikawa</surname>
<given-names>Takashi</given-names></name>
<name><surname>Fujita</surname>
<given-names>Yuki</given-names></name>
<name><surname>Mizusaki</surname>
<given-names>Tomoteru</given-names></name>
<name><surname>Betsuin</surname>
<given-names>Sae</given-names></name>
<name><surname>Takamatsu</surname>
<given-names>Haruki</given-names></name>
<name><surname>Maegawa</surname>
<given-names>Tomohiro</given-names></name>
<name><surname>Monguchi</surname>
<given-names>Yasunari</given-names></name>
<name><surname>Sajiki</surname>
<given-names>Hironao</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>293</fpage>
<lpage>304</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06303k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06303k">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06303k">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis and configuration determination of all enantiopure stereoisomers of the melatonin receptor ligand 4-phenyl-2-propionamidotetralin using an expedient optical resolution of 4-phenyl-2-tetralone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06369c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lucarini</surname>
<given-names>Simone</given-names></name>
<name><surname>Bartolucci</surname>
<given-names>Silvia</given-names></name>
<name><surname>Bedini</surname>
<given-names>Annalida</given-names></name>
<name><surname>Gatti</surname>
<given-names>Giuseppe</given-names></name>
<name><surname>Orlando</surname>
<given-names>Pierfrancesco</given-names></name>
<name><surname>Piersanti</surname>
<given-names>Giovanni</given-names></name>
<name><surname>Spadoni</surname>
<given-names>Gilberto</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>305</fpage>
<lpage>313</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06369c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06369c">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06369c">PDF</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
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<article-meta>
<title-group>
<article-title>Synthesis of luminescent homo-dinuclear cationic lanthanide cyclen complexes bearing amide pendant arms through the use of copper catalysed (1,3-Huisgen, CuAAC) click chemistry</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06203d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Molloy</surname>
<given-names>Jennifer K.</given-names></name>
<name><surname>Kotova</surname>
<given-names>Oxana</given-names></name>
<name><surname>Peacock</surname>
<given-names>Robert D.</given-names></name>
<name><surname>Gunnlaugsson</surname>
<given-names>Thorfinnur</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>314</fpage>
<lpage>322</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06203d">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06203d">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06203d">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tyrosine nitration affects thymidylate synthase properties</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06360j</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dąbrowska-Maś</surname>
<given-names>Elżbieta</given-names></name>
<name><surname>Frączyk</surname>
<given-names>Tomasz</given-names></name>
<name><surname>Ruman</surname>
<given-names>Tomasz</given-names></name>
<name><surname>Radziszewska</surname>
<given-names>Karolina</given-names></name>
<name><surname>Wilk</surname>
<given-names>Piotr</given-names></name>
<name><surname>Cieśla</surname>
<given-names>Joanna</given-names></name>
<name><surname>Zieliński</surname>
<given-names>Zbigniew</given-names></name>
<name><surname>Jurkiewicz</surname>
<given-names>Agata</given-names></name>
<name><surname>Gołos</surname>
<given-names>Barbara</given-names></name>
<name><surname>Wińska</surname>
<given-names>Patrycja</given-names></name>
<name><surname>Wałajtys-Rode</surname>
<given-names>Elżbieta</given-names></name>
<name><surname>Leś</surname>
<given-names>Andrzej</given-names></name>
<name><surname>Nizioł</surname>
<given-names>Joanna</given-names></name>
<name><surname>Jarmuła</surname>
<given-names>Adam</given-names></name>
<name><surname>Stefanowicz</surname>
<given-names>Piotr</given-names></name>
<name><surname>Szewczuk</surname>
<given-names>Zbigniew</given-names></name>
<name><surname>Rode</surname>
<given-names>Wojciech</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>323</fpage>
<lpage>331</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06360j">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06360j">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06360j">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Squaramide-catalyzed enantioselective Michael addition of malononitrile to chalcones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06302b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Yang</surname>
<given-names>Wen</given-names></name>
<name><surname>Jia</surname>
<given-names>Yang</given-names></name>
<name><surname>Du</surname>
<given-names>Da-Ming</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>332</fpage>
<lpage>338</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06302b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06302b">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06302b">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
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<article-meta>
<title-group>
<article-title>Asymmetric α-2-tosylethenylation of &lt;i&gt;N&lt;/i&gt;,&lt;i&gt;N&lt;/i&gt;-dialkyl-l-amino acid esters &lt;i&gt;via&lt;/i&gt; the formation of non-racemic ammonium enolates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06074k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tayama</surname>
<given-names>Eiji</given-names></name>
<name><surname>Igarashi</surname>
<given-names>Tomohito</given-names></name>
<name><surname>Iwamoto</surname>
<given-names>Hajime</given-names></name>
<name><surname>Hasegawa</surname>
<given-names>Eietsu</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>339</fpage>
<lpage>345</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06074k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06074k">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06074k">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
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</journal-meta>
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<title-group>
<article-title>Acidic-functionalized ionic liquid as an efficient, green and reusable catalyst for hetero-Michael addition of nitrogen, sulfur and oxygen nucleophiles to &lt;i&gt;α&lt;/i&gt;,&lt;i&gt;β&lt;/i&gt;-unsaturated ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06346d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Han</surname>
<given-names>Feng</given-names></name>
<name><surname>Yang</surname>
<given-names>Lei</given-names></name>
<name><surname>Li</surname>
<given-names>Zhen</given-names></name>
<name><surname>Xia</surname>
<given-names>Chungu</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>346</fpage>
<lpage>354</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06346d">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06346d">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06346d">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
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</journal-meta>
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<title-group>
<article-title>P/S ligands derived from carbohydrates in Rh-catalyzed hydrosilylation of ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06305g</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khiar</surname>
<given-names>Noureddine</given-names></name>
<name><surname>Leal</surname>
<given-names>Manuel Pernía</given-names></name>
<name><surname>Navas</surname>
<given-names>Raquel</given-names></name>
<name><surname>Moya</surname>
<given-names>Juan Francisco</given-names></name>
<name><surname>Pérez</surname>
<given-names>María Victoria García</given-names></name>
<name><surname>Fernández</surname>
<given-names>Inmaculada</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>355</fpage>
<lpage>360</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06305g">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06305g">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06305g">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
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<title-group>
<article-title>A novel D-ring modified taxoid: synthesis and biological evaluation of a γ-lactone analogue of docetaxel</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06535a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gao</surname>
<given-names>Feng</given-names></name>
<name><surname>Yang</surname>
<given-names>Zhan-Kun</given-names></name>
<name><surname>Chen</surname>
<given-names>Qiao-Hong</given-names></name>
<name><surname>Chen</surname>
<given-names>Xiao-Guang</given-names></name>
<name><surname>Wang</surname>
<given-names>Feng-Peng</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>361</fpage>
<lpage>366</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06535a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06535a">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06535a">PDF</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Lithium amidoborane, a highly chemoselective reagent for the reduction of α,β-unsaturated ketones to allylic alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06368e</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Xu</surname>
<given-names>Weiliang</given-names></name>
<name><surname>Zhou</surname>
<given-names>Yonggui</given-names></name>
<name><surname>Wang</surname>
<given-names>Ruimin</given-names></name>
<name><surname>Wu</surname>
<given-names>Guotao</given-names></name>
<name><surname>Chen</surname>
<given-names>Ping</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>367</fpage>
<lpage>371</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06368e">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06368e">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06368e">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Resorcin[4]arene-derived mono-, bis- and tetra-imidazolium salts as ligand precursors for Suzuki–Miyaura cross-coupling</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06404e</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Moll</surname>
<given-names>Hani El</given-names></name>
<name><surname>Sémeril</surname>
<given-names>David</given-names></name>
<name><surname>Matt</surname>
<given-names>Dominique</given-names></name>
<name><surname>Toupet</surname>
<given-names>Loïc</given-names></name>
<name><surname>Harrowfield</surname>
<given-names>Jean-Jacques</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>372</fpage>
<lpage>382</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06404e">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06404e">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06404e">PDF</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Neuronal growth promoting sesquiterpene–neolignans; syntheses and biological studies</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06363d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cheng</surname>
<given-names>Xu</given-names></name>
<name><surname>Harzdorf</surname>
<given-names>Nicole</given-names></name>
<name><surname>Khaing</surname>
<given-names>Zin</given-names></name>
<name><surname>Kang</surname>
<given-names>Danby</given-names></name>
<name><surname>Camelio</surname>
<given-names>Andrew M.</given-names></name>
<name><surname>Shaw</surname>
<given-names>Travis</given-names></name>
<name><surname>Schmidt</surname>
<given-names>Christine E.</given-names></name>
<name><surname>Siegel</surname>
<given-names>Dionicio</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>383</fpage>
<lpage>393</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06363d">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06363d">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06363d">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Skeletal rearrangements resulting from reactions of 1,6:2,3- and 1,6:3,4-dianhydro-β-d-hexopyranoses with diethylaminosulphur trifluoride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06336g</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Karban</surname>
<given-names>Jindřich</given-names></name>
<name><surname>Císařová</surname>
<given-names>Ivana</given-names></name>
<name><surname>Strašák</surname>
<given-names>Tomáš</given-names></name>
<name><surname>Šťastná</surname>
<given-names>Lucie Červenková</given-names></name>
<name><surname>Sýkora</surname>
<given-names>Jan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>394</fpage>
<lpage>403</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06336g">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06336g">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06336g">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of geminal bisphosphonates &lt;i&gt;via&lt;/i&gt; organocatalyzed enantioselective Michael additions of cyclic ketones and 4-piperidones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06473h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Phillips</surname>
<given-names>Ana Maria Faísca</given-names></name>
<name><surname>Barros</surname>
<given-names>Maria Teresa</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>404</fpage>
<lpage>412</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06473h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06473h">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06473h">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Asymmetric Michael addition reactions of 3-substituted benzofuran-2(3&lt;i&gt;H&lt;/i&gt;)-ones to nitroolefins catalyzed by a bifunctional tertiary-amine thiourea</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06518a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Li</surname>
<given-names>Xin</given-names></name>
<name><surname>Xue</surname>
<given-names>Xiao-Song</given-names></name>
<name><surname>Liu</surname>
<given-names>Cong</given-names></name>
<name><surname>Wang</surname>
<given-names>Bin</given-names></name>
<name><surname>Tan</surname>
<given-names>Bo-Xuan</given-names></name>
<name><surname>Jin</surname>
<given-names>Jia-Lu</given-names></name>
<name><surname>Zhang</surname>
<given-names>Yue-Yan</given-names></name>
<name><surname>Dong</surname>
<given-names>Nan</given-names></name>
<name><surname>Cheng</surname>
<given-names>Jin-Pei</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>413</fpage>
<lpage>420</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06518a">Abstract</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Discovering potent inhibitors against c-Met kinase: molecular design, organic synthesis and bioassay</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06186k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Liang</surname>
<given-names>Zhongjie</given-names></name>
<name><surname>Ding</surname>
<given-names>Xiao</given-names></name>
<name><surname>Ai</surname>
<given-names>Jing</given-names></name>
<name><surname>Kong</surname>
<given-names>Xiangqian</given-names></name>
<name><surname>Chen</surname>
<given-names>Limin</given-names></name>
<name><surname>Chen</surname>
<given-names>Liang</given-names></name>
<name><surname>Luo</surname>
<given-names>Cheng</given-names></name>
<name><surname>Geng</surname>
<given-names>Meiyu</given-names></name>
<name><surname>Liu</surname>
<given-names>Hong</given-names></name>
<name><surname>Chen</surname>
<given-names>Kaixian</given-names></name>
<name><surname>Jiang</surname>
<given-names>Hualiang</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>421</fpage>
<lpage>430</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06186k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06186k">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06186k">PDF</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enantioselective organocatalytic oxyamination of unprotected 3-substituted oxindoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06503c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Companyó</surname>
<given-names>Xavier</given-names></name>
<name><surname>Valero</surname>
<given-names>Guillem</given-names></name>
<name><surname>Pineda</surname>
<given-names>Oriol</given-names></name>
<name><surname>Calvet</surname>
<given-names>Teresa</given-names></name>
<name><surname>Font-Bardía</surname>
<given-names>Mercè</given-names></name>
<name><surname>Moyano</surname>
<given-names>Albert</given-names></name>
<name><surname>Rios</surname>
<given-names>Ramon</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>431</fpage>
<lpage>439</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06503c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06503c">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06503c">PDF</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemo-enzymatic syntheses of drimane-type sesquiterpenes and the fundamental core of hongoquercin meroterpenoid by recombinant squalene–hopene cyclase</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06419c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Yonemura</surname>
<given-names>Yukie</given-names></name>
<name><surname>Ohyama</surname>
<given-names>Takuro</given-names></name>
<name><surname>Hoshino</surname>
<given-names>Tsutomu</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>440</fpage>
<lpage>446</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06419c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06419c">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06419c">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of functionalized tetrahydro-1,3-diazepin-2-ones and 1-carbamoyl-1&lt;i&gt;H&lt;/i&gt;-pyrroles &lt;i&gt;via&lt;/i&gt; ring expansion and ring expansion/ring contraction of tetrahydropyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob06284k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fesenko</surname>
<given-names>Anastasia A.</given-names></name>
<name><surname>Trafimova</surname>
<given-names>Ludmila A.</given-names></name>
<name><surname>Shutalev</surname>
<given-names>Anatoly D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>447</fpage>
<lpage>462</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob06284k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2012/OB/c1ob06284k">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2012/OB/c1ob06284k">PDF</self-uri>
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</article>
<article>
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<journal-meta>
<journal-title>Organic &amp;  Biomolecular Chemistry</journal-title>
<issn>1477-0520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Back cover</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1ob90084f</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2012</year></pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>463</fpage>
<lpage>464</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1ob90084f">Abstract</self-uri>
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