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<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>EditorialGreen chemistry in Ireland </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b108143h</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>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>G60</fpage>
<lpage>G60</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=b108143h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2001/GC/b108143h">PDF</self-uri>
</article-meta>
</front>
<article-type>editorial</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>News and ViewsRunning fuel cells on biogas — a renewable fuel Highlights Centre for Green Chemistry, Monash University From plant to plastic, 	 								Renewables are fantastic! </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b108144f</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>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>G61</fpage>
<lpage>G71</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=b108144f">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2001/GC/b108144f">PDF</self-uri>
</article-meta>
</front>
<article-type>news</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sugar-derived building blocks. Part 26. Hydrophilic pyrroles, pyridazines and diazepinones from d-fructose and isomaltulose </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b105630c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lichtenthaler</surname>
<given-names>Frieder W.</given-names></name>
<name><surname>Brust</surname>
<given-names>Andreas</given-names></name>
<name><surname>Cuny</surname>
<given-names>Eckehard</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>201</fpage>
<lpage>209</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=b105630c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2001/GC/b105630c">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2001/GC/b105630c">PDF</self-uri>
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</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Behavior of the solvatochromic probes Reichardt’s dye, pyrene, dansylamide, Nile Red and 1-pyrenecarbaldehyde within the room-temperature ionic liquid bmimPF&lt;sub&gt;6&lt;/sub&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b103592b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fletcher</surname>
<given-names>Kristin A.</given-names></name>
<name><surname>Storey</surname>
<given-names>Isaiah A.</given-names></name>
<name><surname>Hendricks</surname>
<given-names>Ashley E.</given-names></name>
<name><surname>Pandey</surname>
<given-names>Shubha</given-names></name>
<name><surname>Pandey</surname>
<given-names>Siddharth</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>210</fpage>
<lpage>215</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=b103592b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2001/GC/b103592b">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2001/GC/b103592b">PDF</self-uri>
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</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Flow analysis strategies to greener analytical chemistry. An overview </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b103187m</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rocha</surname>
<given-names>Fábio R. P.</given-names></name>
<name><surname>Nóbrega</surname>
<given-names>Joaquim A.</given-names></name>
<name><surname>Filho</surname>
<given-names>Orlando Fatibello</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>216</fpage>
<lpage>220</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=b103187m">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2001/GC/b103187m">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2001/GC/b103187m">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Laser bleaching of cellulosic fabrics by sodium borohydride aqueous solution; a total chlorine free process </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b104429j</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ouchi</surname>
<given-names>Akihiko</given-names></name>
<name><surname>Obata</surname>
<given-names>Toru</given-names></name>
<name><surname>Sakai</surname>
<given-names>Hitoshi</given-names></name>
<name><surname>Sakuragi</surname>
<given-names>Masako</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>221</fpage>
<lpage>223</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=b104429j">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2001/GC/b104429j">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2001/GC/b104429j">PDF</self-uri>
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</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Green photochemistry: the solar-chemical ‘Photo–Friedel–Crafts acylation’ of quinones </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b106425h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Schiel</surname>
<given-names>Christian</given-names></name>
<name><surname>Oelgemöller</surname>
<given-names>Michael</given-names></name>
<name><surname>Ortner</surname>
<given-names>Jürgen</given-names></name>
<name><surname>Mattay</surname>
<given-names>Jochen</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>224</fpage>
<lpage>228</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=b106425h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2001/GC/b106425h">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2001/GC/b106425h">PDF</self-uri>
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</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Water, a clean, inexpensive, and re-usable reaction medium. One-pot synthesis of (&lt;i&gt;E&lt;/i&gt;)-2-aryl-1-cyano-1-nitroethenes </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b105522b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Amantini</surname>
<given-names>D.</given-names></name>
<name><surname>Fringuelli</surname>
<given-names>F.</given-names></name>
<name><surname>Piermatti</surname>
<given-names>O.</given-names></name>
<name><surname>Pizzo</surname>
<given-names>F.</given-names></name>
<name><surname>Vaccaro</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>229</fpage>
<lpage>232</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=b105522b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2001/GC/b105522b">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2001/GC/b105522b">PDF</self-uri>
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</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A single step synthesis of 2-phenylpyridine from acetophenone, ethanol, formaldehyde and ammonia over molecular sieve catalysts </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b106183f</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gopal</surname>
<given-names>D. Venu</given-names></name>
<name><surname>Subrahmanyam</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>233</fpage>
<lpage>237</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=b106183f">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2001/GC/b106183f">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2001/GC/b106183f">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
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</journal-meta>
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<title-group>
<article-title>Low-toxicity red ceramic pigments for porcelainised stoneware from lanthanide–cerianite solid solutions </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b105830b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>García</surname>
<given-names>A.</given-names></name>
<name><surname>Llusar</surname>
<given-names>M.</given-names></name>
<name><surname>Calbo</surname>
<given-names>J.</given-names></name>
<name><surname>Tena</surname>
<given-names>M. A.</given-names></name>
<name><surname>Monrós</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>238</fpage>
<lpage>242</lpage>
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<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2001/GC/b105830b">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2001/GC/b105830b">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
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<title-group>
<article-title>Alumina: a cheap, active and selective catalyst for epoxidations with (aqueous) hydrogen peroxide </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b103952k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Vliet</surname>
<given-names>Michiel C. A. van</given-names></name>
<name><surname>Mandelli</surname>
<given-names>Dalmo</given-names></name>
<name><surname>Arends</surname>
<given-names>Isabel W. C. E.</given-names></name>
<name><surname>Schuchardt</surname>
<given-names>Ulf</given-names></name>
<name><surname>Sheldon</surname>
<given-names>Roger A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>243</fpage>
<lpage>246</lpage>
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<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2001/GC/b103952k">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2001/GC/b103952k">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
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<title-group>
<article-title>Montmorillonite K-10 catalyzed synthesis of β-keto esters: condensation of ethyl diazoacetate with aldehydes under mild conditions </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b104116a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bandgar</surname>
<given-names>B. P.</given-names></name>
<name><surname>Pandit</surname>
<given-names>S. S.</given-names></name>
<name><surname>Sadavarte</surname>
<given-names>V. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>247</fpage>
<lpage>249</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=b104116a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2001/GC/b104116a">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2001/GC/b104116a">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
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<title-group>
<article-title>Use of water as a direct hydrogen donor in supercritical carbon dioxide: a novel and efficient Zn–H&lt;sub&gt;2&lt;/sub&gt;O–CO&lt;sub&gt;2&lt;/sub&gt; system for selective reduction of aldehydes to alcohols </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b105307h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Li</surname>
<given-names>Guoping</given-names></name>
<name><surname>Jiang</surname>
<given-names>Huanfeng</given-names></name>
<name><surname>Li</surname>
<given-names>Jinheng</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>250</fpage>
<lpage>251</lpage>
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<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2001/GC/b105307h">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2001/GC/b105307h">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
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<title-group>
<article-title>Solvent-free reactions of solid substances using solid catalysts: estimation of physical states of substrate–product mixtures by the BET method and the SEM observation </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b106031g</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kitamura</surname>
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<name><surname>Harada</surname>
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</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>252</fpage>
<lpage>256</lpage>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
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<title-group>
<article-title>Layered double hydroxide fluoride: a novel solid base catalyst for C–C bond formation </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b107124f</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Choudary</surname>
<given-names>B. M.</given-names></name>
<name><surname>Kantam</surname>
<given-names>M. Lakshmi</given-names></name>
<name><surname>Neeraja</surname>
<given-names>V.</given-names></name>
<name><surname>Rao</surname>
<given-names>K. Koteswara</given-names></name>
<name><surname>Figueras</surname>
<given-names>F.</given-names></name>
<name><surname>Delmotte</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>257</fpage>
<lpage>260</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=b107124f">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2001/GC/b107124f">HTML</self-uri><self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/2001/GC/b107124f">PDF</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
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<title-group>
<article-title>Potassium fluoride doped alumina: an effective reagent for ester hydrolysis under solvent free conditions </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b106423c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kabalka</surname>
<given-names>George W.</given-names></name>
<name><surname>Wang</surname>
<given-names>Lei</given-names></name>
<name><surname>Pagni</surname>
<given-names>Richard M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>261</fpage>
<lpage>262</lpage>
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<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
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<article-meta>
<title-group>
<article-title>Microwave mediated solvent-free acetylation of deactivated and hindered phenols </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b107696p</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Deka</surname>
<given-names>Nabajyoti</given-names></name>
<name><surname>Mariotte</surname>
<given-names>Anne-Marie</given-names></name>
<name><surname>Boumendjel</surname>
<given-names>Ahcène</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>263</fpage>
<lpage>264</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=b107696p">Abstract</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Green Chemistry</journal-title>
<issn>1463-9262</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organic reactions in aqueous medium: FeF&lt;sub&gt;3&lt;/sub&gt; catalyzed chemoselective addition of cyanotrimethylsilane to aldehydes </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/b106872p</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bandgar</surname>
<given-names>B. P.</given-names></name>
<name><surname>Kamble</surname>
<given-names>V. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2001</year></pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>265</fpage>
<lpage>266</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=b106872p">Abstract</self-uri>
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