<?xml version="1.0" encoding="utf-8"?>
<articles xmlns:xlink="http://www.w3.org/1999/xlink">
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
The efficacy of ‘Claycop’ in the dinitration of
toluene
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a701226h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lancaster</surname>
<given-names>N. Llewellyn</given-names></name>
<name><surname>Moodie</surname>
<given-names>Roy B.</given-names></name>
<name><surname>Sandall</surname>
<given-names>John P. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>847</fpage>
<lpage>848</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a701226h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a701226h">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
The kinetically-controlled Cope rearrangement of
2,5-bis(4-methoxyphenyl)hexa-1,5-dienes induced by photosensitised
electron transfer
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a701043e</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ikeda</surname>
<given-names>Hiroshi</given-names></name>
<name><surname>Ishida</surname>
<given-names>Akito</given-names></name>
<name><surname>Takasaki</surname>
<given-names>Toshihiko</given-names></name>
<name><surname>Tojo</surname>
<given-names>Sachiko</given-names></name>
<name><surname>Takamuku</surname>
<given-names>Setsuo</given-names></name>
<name><surname>Miyashi</surname>
<given-names>Tsutomu</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>849</fpage>
<lpage>850</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a701043e">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a701043e">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Structure–reactivity relationships in the rate of esterification
by acetylimidazole: the influence of the second hydroxy group and of the
length of the
N-ω-hydroxy-n-alkyl chain in
3-(N-methyl,
N-ω-hydroxy-n-alkyl)amino-2-
tert-butylpropan-1-ols
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a608033b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Madder</surname>
<given-names>Annemieke</given-names></name>
<name><surname>Clercq</surname>
<given-names>Pierre J. De</given-names></name>
<name><surname>Maskill</surname>
<given-names>Howard</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>851</fpage>
<lpage>852</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a608033b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a608033b">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Aryl vinyl sulfides as probes for electrophilic versus
electron
transfer mechanisms
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a605317c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aplin</surname>
<given-names>J. Todd</given-names></name>
<name><surname>Bauld</surname>
<given-names>Nathan L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>853</fpage>
<lpage>855</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a605317c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a605317c">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Gaseous and crystalline phase molecular structures of
4,6-dichloropyrimidine, 2,6-dichloropyrazine and 3,6-dichloropyridazine
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a700069c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Morrison</surname>
<given-names>Carole A.</given-names></name>
<name><surname>Smart</surname>
<given-names>Bruce A.</given-names></name>
<name><surname>Parsons</surname>
<given-names>Simon</given-names></name>
<name><surname>Brown</surname>
<given-names>Ewan M.</given-names></name>
<name><surname>Rankin</surname>
<given-names>David W. H.</given-names></name>
<name><surname>Robertson</surname>
<given-names>Heather E.</given-names></name>
<name><surname>Miller</surname>
<given-names>Jennifer</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>857</fpage>
<lpage>868</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a700069c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a700069c">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
The structure and intermolecular interactions of a creatinine
designed–receptor complex, studied by ab initio
methods
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a608586e</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Craw</surname>
<given-names>J. Simon</given-names></name>
<name><surname>Cooper</surname>
<given-names>Matthew D.</given-names></name>
<name><surname>Hillier</surname>
<given-names>Ian H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>869</fpage>
<lpage>872</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a608586e">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a608586e">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Thermodynamics of gas phase proton transfer reactions involving
substituted benzaldehydes
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a608287d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>Peter D. J.</given-names></name>
<name><surname>Fernandez</surname>
<given-names>M. Tereza</given-names></name>
<name><surname>Pocsfalvi</surname>
<given-names>Gabriella</given-names></name>
<name><surname>Mason</surname>
<given-names>Rod S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>873</fpage>
<lpage>880</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a608287d">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a608287d">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Proton chemical shifts in NMR. Part 9.1 Steric
and electric field effects in chlorine substituent chemical shifts (SCS)
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a608095b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abraham</surname>
<given-names>Raymond J.</given-names></name>
<name><surname>Warne</surname>
<given-names>Mark A.</given-names></name>
<name><surname>Griffiths</surname>
<given-names>Lee</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>881</fpage>
<lpage>886</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a608095b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a608095b">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
New insights into N-tert-butyl-α-phenylnitrone
(PBN) as a spin trap. Part 2.&lt;sup&gt;1&lt;/sup&gt; The
reactivity
of PBN and 5,5-dimethyl-4,5-dihydropyrrole N-oxide
(DMPO) toward N-heteroaromatic bases
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a608004i</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alberti</surname>
<given-names>Angelo</given-names></name>
<name><surname>Carloni</surname>
<given-names>Patricia</given-names></name>
<name><surname>Eberson</surname>
<given-names>Lennart</given-names></name>
<name><surname>Greci</surname>
<given-names>Lucedio</given-names></name>
<name><surname>Stipa</surname>
<given-names>Pierluigi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>887</fpage>
<lpage>892</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a608004i">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a608004i">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Fluoro spin adducts and their modes of formation
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a607509f</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eberson</surname>
<given-names>Lennart</given-names></name>
<name><surname>Persson</surname>
<given-names>Ola</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>893</fpage>
<lpage>898</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a607509f">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a607509f">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Solid state NMR, IR and X-ray diffraction studies of the structure and
motion of L-leucinamide
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a607971g</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wang</surname>
<given-names>Yulan</given-names></name>
<name><surname>Belton</surname>
<given-names>Peter S.</given-names></name>
<name><surname>Tang</surname>
<given-names>Huiru</given-names></name>
<name><surname>Wellner</surname>
<given-names>Nikolaus</given-names></name>
<name><surname>Davies</surname>
<given-names>Sian C.</given-names></name>
<name><surname>Hughes</surname>
<given-names>David L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>899</fpage>
<lpage>904</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a607971g">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a607971g">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Understanding conformer equilibria in solution with the aid of
calculated &lt;sup&gt;13&lt;/sup&gt;C NMR spectra.&lt;sup&gt;1&lt;/sup&gt; A density functional
and molecular mechanics study
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a607921k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Stahl</surname>
<given-names>Martin</given-names></name>
<name><surname>Schopfer</surname>
<given-names>Ulrich</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>905</fpage>
<lpage>908</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a607921k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a607921k">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Some reactions of ammonia and primary amines with propanal,
2-chloroethanal, 2,2-dichloroethanal and 2,2,2-trichloroethanal in
acetonitrile
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a607869i</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crampton</surname>
<given-names>Michael R.</given-names></name>
<name><surname>Lord</surname>
<given-names>Simon D.</given-names></name>
<name><surname>Millar</surname>
<given-names>Ross</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>909</fpage>
<lpage>916</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a607869i">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a607869i">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Photolysis of some N-nitroso- and
N-nitro-anilines in solution
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a607823k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gowenlock</surname>
<given-names>Brian G.</given-names></name>
<name><surname>Pfab</surname>
<given-names>Josef</given-names></name>
<name><surname>Young</surname>
<given-names>Victor M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>915</fpage>
<lpage>920</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a607823k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a607823k">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
The structure of diphosphaallenic radical cations as evidenced by EPR
experiments and ab initio calculations
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a607742k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chentit</surname>
<given-names>Mostafa</given-names></name>
<name><surname>Sidorenkova</surname>
<given-names>Helena</given-names></name>
<name><surname>Jouaiti</surname>
<given-names>Abdelaziz</given-names></name>
<name><surname>Terron</surname>
<given-names>Gustavo</given-names></name>
<name><surname>Geoffroy</surname>
<given-names>Michel</given-names></name>
<name><surname>Ellinger</surname>
<given-names>Yves</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>921</fpage>
<lpage>926</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a607742k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a607742k">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Conformational analysis of 3,3′-, 3,4′- and
4,4′-dimethoxy-2,2′-bithiophenes as models for related
polymers
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a607644k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bongini</surname>
<given-names>Alessandro</given-names></name>
<name><surname>Brioni</surname>
<given-names>Federica</given-names></name>
<name><surname>Panunzio</surname>
<given-names>Mauro</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>927</fpage>
<lpage>930</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a607644k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a607644k">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Electrochemical and spectroscopic properties of a series of
tert-butyl-substituted para-extended
quinones
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a607113i</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Zhou</surname>
<given-names>Jinkui</given-names></name>
<name><surname>Rieker</surname>
<given-names>Anton</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>931</fpage>
<lpage>938</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a607113i">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a607113i">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
The theoretical basis of the isoinversion principle
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606888j</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gypser</surname>
<given-names>Andreas</given-names></name>
<name><surname>Norrby</surname>
<given-names>Per-Ola</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>939</fpage>
<lpage>944</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606888j">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606888j">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Intramolecular
O–H · · · O
hydrogen
bonds assisted by resonance. Correlation between crystallographic data
and &lt;sup&gt;1&lt;/sup&gt;H NMR chemical shifts
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606862f</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bertolasi</surname>
<given-names>Valerio</given-names></name>
<name><surname>Gilli</surname>
<given-names>Paola</given-names></name>
<name><surname>Ferretti</surname>
<given-names>Valeria</given-names></name>
<name><surname>Gilli</surname>
<given-names>Gastone</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>945</fpage>
<lpage>952</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606862f">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606862f">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Ring strain energy and enthalpy of formation of oxiranone: an
ab initio theoretical determination
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606820k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rodriquez</surname>
<given-names>Christopher F.</given-names></name>
<name><surname>Williams</surname>
<given-names>Ian H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>953</fpage>
<lpage>958</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606820k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606820k">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Ab initio theoretical investigation of the mechanism
for α-lactone formation from α-halocarboxylates: leaving
group, substituent, solvent and isotope effects
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606819g</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rodriquez</surname>
<given-names>Christopher F.</given-names></name>
<name><surname>Williams</surname>
<given-names>Ian H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>959</fpage>
<lpage>966</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606819g">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606819g">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
One-pot stereoselective synthesis of (Z)-diethyl
α-chlorovinylphosphonates
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606713a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Perlikowska</surname>
<given-names>Wieslawa</given-names></name>
<name><surname>Mphahlele</surname>
<given-names>Malose J.</given-names></name>
<name><surname>Modro</surname>
<given-names>Tomasz A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>967</fpage>
<lpage>970</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606713a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606713a">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Rates of thermolysis of azidobenzenes in solution: large stabilizations
of transition states by charge transfer from electron-donor substituents
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606704b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dyall</surname>
<given-names>Leonard K.</given-names></name>
<name><surname>L’abbé</surname>
<given-names>Gerrit</given-names></name>
<name><surname>Dehaen</surname>
<given-names>Wim</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>971</fpage>
<lpage>976</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606704b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606704b">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
A new kinetic model for the acid-catalysed reactions of
N-(2-aminophenyl)phthalamic acid in aqueous media
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606699b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Perry</surname>
<given-names>Christopher J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>977</fpage>
<lpage>982</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606699b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606699b">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Reactions of carbonyl compounds in basic solutions. Part
23.1 The mechanism of the base-catalysed ring
fission of 2,2-dihydroxyindane-1,3-diones
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606312h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>Keith</given-names></name>
<name><surname>Rumpal</surname>
<given-names>Sanjay</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>983</fpage>
<lpage>988</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606312h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606312h">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Reactions of carbonyl compounds in basic solutions. Part
24.1 The mechanism of the base-catalysed ring
fission of substituted benzocyclobutene-1,2-diones
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606310a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>Keith</given-names></name>
<name><surname>Horri</surname>
<given-names>M. Vahid</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>989</fpage>
<lpage>992</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606310a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606310a">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Reactions of carbonyl compounds in basic solutions. Part
25.1 The mechanism of the base-catalysed ring
fission of 3,4-diphenylcyclobut-3-ene-1,2-diones
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606412d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Al-Najjar</surname>
<given-names>Abdulaziz</given-names></name>
<name><surname>Bowden</surname>
<given-names>Keith</given-names></name>
<name><surname>Horri</surname>
<given-names>M. Vahid</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>993</fpage>
<lpage>996</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606412d">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606412d">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Reactions of carbonyl compounds in basic solutions. Part 26.&lt;sup&gt;1&lt;/sup&gt;
The mechanisms of the base-catalysed cyclisation of 1,2-diacetylbenzene,
1,8-diacetylnaphthalene, 4,5-diacetylphenanthrene and
2,2′-diacetylbiphenyl
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606399c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>Keith</given-names></name>
<name><surname>Brownhill</surname>
<given-names>Andrew</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>997</fpage>
<lpage>1002</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606399c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606399c">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
GIAO-SCF calculation of the chemical shifts in simple enamines. A
comparison of theory with experiment
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606273c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Weston</surname>
<given-names>Jennie</given-names></name>
<name><surname>Ahlbrecht</surname>
<given-names>Hubertus</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>1003</fpage>
<lpage>1006</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606273c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606273c">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Photoinduced electron transfer from tetraethoxyethene to C&lt;sub&gt;60&lt;/sub&gt;
and C&lt;sub&gt;70&lt;/sub&gt; studied by laser flash photolysis
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606244j</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ito</surname>
<given-names>Osamu</given-names></name>
<name><surname>Sasaki</surname>
<given-names>Yoshiko</given-names></name>
<name><surname>Watanabe</surname>
<given-names>Akira</given-names></name>
<name><surname>Hoffmann</surname>
<given-names>Ralf</given-names></name>
<name><surname>Siedschlag</surname>
<given-names>Christina</given-names></name>
<name><surname>Mattay</surname>
<given-names>Jochen</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>1007</fpage>
<lpage>1012</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606244j">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606244j">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
The effect of alcohols on the basic cleavage of
m-nitrophenyl hexanoate by β-cyclodextrin:
allosteric reaction mode switching
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606097h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tee</surname>
<given-names>Oswald S.</given-names></name>
<name><surname>Giorgi</surname>
<given-names>Javier B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>1013</fpage>
<lpage>1018</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606097h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606097h">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Ambident reactivity of aryloxide ions towards the super-electrophile,
4,6-dinitrobenzofuroxan. Kinetics, thermodynamics and stereoelectronic
factors on regioselectivity
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a605907d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buncel</surname>
<given-names>Erwin</given-names></name>
<name><surname>Manderville</surname>
<given-names>Richard A.</given-names></name>
<name><surname>Dust</surname>
<given-names>Julian M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>1019</fpage>
<lpage>1026</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a605907d">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a605907d">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
An unstrained homoallylic secondary adamantyl
toluene-p-sulfonate solvolyses with σ-bond
migration to give a protoadamantyl substituted allylic carbenium
ion
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a605593a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Huang</surname>
<given-names>Xicai</given-names></name>
<name><surname>Bennet</surname>
<given-names>Andrew J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>1027</fpage>
<lpage>1034</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a605593a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a605593a">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Conformational isomerism of phenolic procyanidins: preferred
conformations in organic solvents and water
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a605592c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hatano</surname>
<given-names>Tsutomu</given-names></name>
<name><surname>Hemingway</surname>
<given-names>Richard W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>1035</fpage>
<lpage>1044</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a605592c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a605592c">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Spiro-λ&lt;sup&gt;4&lt;/sup&gt;-sulfanes with O-ligands of different
electronegativity in axial positions. A comparison of
CH&lt;sub&gt;2&lt;/sub&gt;O–S&lt;sup&gt;IV&lt;/sup&gt;–OCO and
CH&lt;sub&gt;2&lt;/sub&gt;O–S&lt;sup&gt;+IV&lt;/sup&gt; · ·
 · OC bond systems
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a604157d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Szabó</surname>
<given-names>Dénes</given-names></name>
<name><surname>Kapovits</surname>
<given-names>István</given-names></name>
<name><surname>Argay</surname>
<given-names>Gyula</given-names></name>
<name><surname>Czugler</surname>
<given-names>Mátyás</given-names></name>
<name><surname>Kálmán</surname>
<given-names>Alajos</given-names></name>
<name><surname>Koritsánszky</surname>
<given-names>Tibor</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>1045</fpage>
<lpage>1054</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a604157d">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a604157d">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
On the solvatochromic reversal of merocyanine dyes. Part
2.1 An experimental and semi-empirical study
of the solvatochromism of α- and γ-vinylogous pyridones
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a605966j</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aliaga</surname>
<given-names>Carolina</given-names></name>
<name><surname>Galdames</surname>
<given-names>Juan Soto</given-names></name>
<name><surname>Rezende</surname>
<given-names>Marcos Caroli</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>5</issue>
<fpage>1055</fpage>
<lpage>1058</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a605966j">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a605966j">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
</articles>
