ChemInform Abstract: Synthesis of Highly Functionalized Pyrrolidines as Tunable Templates for the Direct Access to (.+‐.)‐Coerulescine and the Tricyclic Core of Martinellines.
Identifieur interne : 000516 ( Main/Exploration ); précédent : 000515; suivant : 000517ChemInform Abstract: Synthesis of Highly Functionalized Pyrrolidines as Tunable Templates for the Direct Access to (.+‐.)‐Coerulescine and the Tricyclic Core of Martinellines.
Auteurs : Ronan Le Goff ; Ata Martin Lawson ; Adam Daich ; Sebastien ComesseSource :
- ChemInform [ 0931-7597 ] ; 2013-07-30.
English descriptors
- KwdEn :
Abstract
A series of tetrasubstituted pyrrolidines is synthesized by an aza‐Michael induced ring‐closure tandem reaction of bromide (II) with Michael acceptors (I), (IV), and (VI).
Url:
DOI: 10.1002/chin.201331112
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 000057
- to stream Istex, to step Curation: 000057
- to stream Istex, to step Checkpoint: 000034
- to stream Main, to step Merge: 000515
- to stream Main, to step Curation: 000516
Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">ChemInform Abstract: Synthesis of Highly Functionalized Pyrrolidines as Tunable Templates for the Direct Access to (.+‐.)‐Coerulescine and the Tricyclic Core of Martinellines.</title>
<author><name sortKey="Le Goff, Ronan" sort="Le Goff, Ronan" uniqKey="Le Goff R" first="Ronan" last="Le Goff">Ronan Le Goff</name>
</author>
<author><name sortKey="Lawson, Ata Martin" sort="Lawson, Ata Martin" uniqKey="Lawson A" first="Ata Martin" last="Lawson">Ata Martin Lawson</name>
</author>
<author><name sortKey="Daich, Adam" sort="Daich, Adam" uniqKey="Daich A" first="Adam" last="Daich">Adam Daich</name>
</author>
<author><name sortKey="Comesse, Sebastien" sort="Comesse, Sebastien" uniqKey="Comesse S" first="Sebastien" last="Comesse">Sebastien Comesse</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:5D988E5AA7F21D0DB2C5EE5C129ACB1186CFC224</idno>
<date when="2013" year="2013">2013</date>
<idno type="doi">10.1002/chin.201331112</idno>
<idno type="url">https://api.istex.fr/document/5D988E5AA7F21D0DB2C5EE5C129ACB1186CFC224/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000057</idno>
<idno type="wicri:Area/Istex/Curation">000057</idno>
<idno type="wicri:Area/Istex/Checkpoint">000034</idno>
<idno type="wicri:doubleKey">0931-7597:2013:Le Goff R:cheminform:abstract:synthesis</idno>
<idno type="wicri:Area/Main/Merge">000515</idno>
<idno type="wicri:Area/Main/Curation">000516</idno>
<idno type="wicri:Area/Main/Exploration">000516</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">ChemInform Abstract: Synthesis of Highly Functionalized Pyrrolidines as Tunable Templates for the Direct Access to (.+‐.)‐Coerulescine and the Tricyclic Core of Martinellines.</title>
<author><name sortKey="Le Goff, Ronan" sort="Le Goff, Ronan" uniqKey="Le Goff R" first="Ronan" last="Le Goff">Ronan Le Goff</name>
<affiliation><wicri:noCountry code="subField">Fr.</wicri:noCountry>
</affiliation>
</author>
<author><name sortKey="Lawson, Ata Martin" sort="Lawson, Ata Martin" uniqKey="Lawson A" first="Ata Martin" last="Lawson">Ata Martin Lawson</name>
<affiliation><wicri:noCountry code="subField">Fr.</wicri:noCountry>
</affiliation>
</author>
<author><name sortKey="Daich, Adam" sort="Daich, Adam" uniqKey="Daich A" first="Adam" last="Daich">Adam Daich</name>
<affiliation><wicri:noCountry code="subField">Fr.</wicri:noCountry>
</affiliation>
</author>
<author><name sortKey="Comesse, Sebastien" sort="Comesse, Sebastien" uniqKey="Comesse S" first="Sebastien" last="Comesse">Sebastien Comesse</name>
<affiliation><wicri:noCountry code="subField">Fr.</wicri:noCountry>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">ChemInform</title>
<title level="j" type="abbrev">ChemInform</title>
<idno type="ISSN">0931-7597</idno>
<idno type="eISSN">1522-2667</idno>
<imprint><publisher>WILEY‐VCH Verlag</publisher>
<pubPlace>Weinheim</pubPlace>
<date type="published" when="2013-07-30">2013-07-30</date>
<biblScope unit="volume">44</biblScope>
<biblScope unit="issue">31</biblScope>
</imprint>
<idno type="ISSN">0931-7597</idno>
</series>
<idno type="istex">5D988E5AA7F21D0DB2C5EE5C129ACB1186CFC224</idno>
<idno type="DOI">10.1002/chin.201331112</idno>
<idno type="ArticleID">CHIN201331112</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0931-7597</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>fused pyridine derivatives</term>
<term>fused pyrrole derivatives</term>
<term>pyrrole derivatives</term>
<term>ring closure reactions</term>
<term>spirocyclic compounds</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">A series of tetrasubstituted pyrrolidines is synthesized by an aza‐Michael induced ring‐closure tandem reaction of bromide (II) with Michael acceptors (I), (IV), and (VI).</div>
</front>
</TEI>
<affiliations><list></list>
<tree><noCountry><name sortKey="Comesse, Sebastien" sort="Comesse, Sebastien" uniqKey="Comesse S" first="Sebastien" last="Comesse">Sebastien Comesse</name>
<name sortKey="Daich, Adam" sort="Daich, Adam" uniqKey="Daich A" first="Adam" last="Daich">Adam Daich</name>
<name sortKey="Lawson, Ata Martin" sort="Lawson, Ata Martin" uniqKey="Lawson A" first="Ata Martin" last="Lawson">Ata Martin Lawson</name>
<name sortKey="Le Goff, Ronan" sort="Le Goff, Ronan" uniqKey="Le Goff R" first="Ronan" last="Le Goff">Ronan Le Goff</name>
</noCountry>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/France/explor/LeHavreV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000516 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000516 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/France |area= LeHavreV1 |flux= Main |étape= Exploration |type= RBID |clé= ISTEX:5D988E5AA7F21D0DB2C5EE5C129ACB1186CFC224 |texte= ChemInform Abstract: Synthesis of Highly Functionalized Pyrrolidines as Tunable Templates for the Direct Access to (.+‐.)‐Coerulescine and the Tricyclic Core of Martinellines. }}
This area was generated with Dilib version V0.6.25. |