ChemInform Abstract: Can an Aromatic Ring Alter the Reactions of a Nearby Unsaturated Imide? A Study of the Rate and Selectivity of Nitrile Oxide Cycloaddition Reactions of Acryloyl Derivatives of the Rebek Imide Benzoxazole.
Identifieur interne : 00B734 ( Main/Curation ); précédent : 00B733; suivant : 00B735ChemInform Abstract: Can an Aromatic Ring Alter the Reactions of a Nearby Unsaturated Imide? A Study of the Rate and Selectivity of Nitrile Oxide Cycloaddition Reactions of Acryloyl Derivatives of the Rebek Imide Benzoxazole.
Auteurs : D. P. Curran [États-Unis] ; M. Yoon [États-Unis]Source :
- ChemInform [ 0931-7597 ] ; 1997-05-20.
English descriptors
- KwdEn :
- Acryloyl, Acryloyl derivatives, Aromatic ring, Benzoxazole, Chem, Curran, Cycloaddition, Cycloaddition reactions cycloaddition reactions, Imide, Model imides, Nitrile, Nitrile oxide cycloaddition reactions, Rebek, Rebek imide benzoxazole, Regio, Stereoselectivities, Tetrahedron, Title benzoxazole imides, Univ, Yoon.
- Teeft :
- Acryloyl, Acryloyl derivatives, Aromatic ring, Benzoxazole, Chem, Curran, Cycloaddition, Cycloaddition reactions cycloaddition reactions, Imide, Model imides, Nitrile, Nitrile oxide cycloaddition reactions, Rebek, Rebek imide benzoxazole, Regio, Stereoselectivities, Tetrahedron, Title benzoxazole imides, Univ, Yoon.
Abstract
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Url:
DOI: 10.1002/chin.199721043
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: Pour aller vers cette notice dans l'étape Curation :001607
- to stream Istex, to step Curation: Pour aller vers cette notice dans l'étape Curation :001607
- to stream Istex, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :002D88
- to stream Main, to step Merge: Pour aller vers cette notice dans l'étape Curation :00BF02
Links to Exploration step
ISTEX:5FF1D2850549939E88313AA46A667AD03AF79421Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">ChemInform Abstract: Can an Aromatic Ring Alter the Reactions of a Nearby Unsaturated Imide? A Study of the Rate and Selectivity of Nitrile Oxide Cycloaddition Reactions of Acryloyl Derivatives of the Rebek Imide Benzoxazole.</title>
<author><name sortKey="Curran, D P" sort="Curran, D P" uniqKey="Curran D" first="D. P." last="Curran">D. P. Curran</name>
</author>
<author><name sortKey="Yoon, M" sort="Yoon, M" uniqKey="Yoon M" first="M." last="Yoon">M. Yoon</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:5FF1D2850549939E88313AA46A667AD03AF79421</idno>
<date when="1997" year="1997">1997</date>
<idno type="doi">10.1002/chin.199721043</idno>
<idno type="url">https://api.istex.fr/document/5FF1D2850549939E88313AA46A667AD03AF79421/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">001607</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001607</idno>
<idno type="wicri:Area/Istex/Curation">001607</idno>
<idno type="wicri:Area/Istex/Checkpoint">002D88</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">002D88</idno>
<idno type="wicri:doubleKey">0931-7597:1997:Curran D:cheminform:abstract:can</idno>
<idno type="wicri:Area/Main/Merge">00BF02</idno>
<idno type="wicri:Area/Main/Curation">00B734</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">ChemInform Abstract: Can an Aromatic Ring Alter the Reactions of a Nearby Unsaturated Imide? A Study of the Rate and Selectivity of Nitrile Oxide Cycloaddition Reactions of Acryloyl Derivatives of the Rebek Imide Benzoxazole.</title>
<author><name sortKey="Curran, D P" sort="Curran, D P" uniqKey="Curran D" first="D. P." last="Curran">D. P. Curran</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260</wicri:regionArea>
<placeName><region type="state">Pennsylvanie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Yoon, M" sort="Yoon, M" uniqKey="Yoon M" first="M." last="Yoon">M. Yoon</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260</wicri:regionArea>
<placeName><region type="state">Pennsylvanie</region>
</placeName>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j" type="main">ChemInform</title>
<title level="j" type="alt">CHEMINFORM</title>
<idno type="ISSN">0931-7597</idno>
<idno type="eISSN">1522-2667</idno>
<imprint><biblScope unit="vol">28</biblScope>
<biblScope unit="issue">21</biblScope>
<biblScope unit="page" from="no">no</biblScope>
<biblScope unit="page" to="no">no</biblScope>
<biblScope unit="page-count">1</biblScope>
<publisher>WILEY‐VCH Verlag</publisher>
<pubPlace>Weinheim</pubPlace>
<date type="published" when="1997-05-20">1997-05-20</date>
</imprint>
<idno type="ISSN">0931-7597</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0931-7597</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acryloyl</term>
<term>Acryloyl derivatives</term>
<term>Aromatic ring</term>
<term>Benzoxazole</term>
<term>Chem</term>
<term>Curran</term>
<term>Cycloaddition</term>
<term>Cycloaddition reactions cycloaddition reactions</term>
<term>Imide</term>
<term>Model imides</term>
<term>Nitrile</term>
<term>Nitrile oxide cycloaddition reactions</term>
<term>Rebek</term>
<term>Rebek imide benzoxazole</term>
<term>Regio</term>
<term>Stereoselectivities</term>
<term>Tetrahedron</term>
<term>Title benzoxazole imides</term>
<term>Univ</term>
<term>Yoon</term>
</keywords>
<keywords scheme="Teeft" xml:lang="en"><term>Acryloyl</term>
<term>Acryloyl derivatives</term>
<term>Aromatic ring</term>
<term>Benzoxazole</term>
<term>Chem</term>
<term>Curran</term>
<term>Cycloaddition</term>
<term>Cycloaddition reactions cycloaddition reactions</term>
<term>Imide</term>
<term>Model imides</term>
<term>Nitrile</term>
<term>Nitrile oxide cycloaddition reactions</term>
<term>Rebek</term>
<term>Rebek imide benzoxazole</term>
<term>Regio</term>
<term>Stereoselectivities</term>
<term>Tetrahedron</term>
<term>Title benzoxazole imides</term>
<term>Univ</term>
<term>Yoon</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.</div>
</front>
</TEI>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Amérique/explor/PittsburghV1/Data/Main/Curation
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 00B734 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Curation/biblio.hfd -nk 00B734 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Amérique |area= PittsburghV1 |flux= Main |étape= Curation |type= RBID |clé= ISTEX:5FF1D2850549939E88313AA46A667AD03AF79421 |texte= ChemInform Abstract: Can an Aromatic Ring Alter the Reactions of a Nearby Unsaturated Imide? A Study of the Rate and Selectivity of Nitrile Oxide Cycloaddition Reactions of Acryloyl Derivatives of the Rebek Imide Benzoxazole. }}
This area was generated with Dilib version V0.6.38. |