N‐Acyliminium Ion Chemistry: Highly Efficient and Versatile Carbon–Carbon Bond Formation by Nucleophilic Substitution of Hydroxy Groups Catalyzed by Sn(NTf2)4
Identifieur interne : 000995 ( Main/Exploration ); précédent : 000994; suivant : 000996N‐Acyliminium Ion Chemistry: Highly Efficient and Versatile Carbon–Carbon Bond Formation by Nucleophilic Substitution of Hydroxy Groups Catalyzed by Sn(NTf2)4
Auteurs : Raja Ben Thman [Tunisie] ; Radouane Affani ; Marie-José Tranchant ; Sylvain Antoniotti ; Vincent Dalla [France] ; Elisabet Du Ach [France]Source :
- Angewandte Chemie [ 0044-8249 ] ; 2010-01-18.
English descriptors
- KwdEn :
Abstract
Atomökonomisch: Nichtmodifizierte N,O‐Halbacetale wurden in einer katalytischen, hocheffizienten α‐Amidoalkylierung kohlenstoffzentrierter Nucleophile eingesetzt, darunter Siliciumverbindungen, aktive Methylenderivate, elektronenreiche Arene und selbst einfache Ketone (siehe Schema). In der Regel genügt 1 Mol‐% des supersauren Lewis‐Reagens Sn(NTf2)4 als Katalysator.
Url:
DOI: 10.1002/ange.200906036
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 000479
- to stream Istex, to step Curation: 000479
- to stream Istex, to step Checkpoint: 000179
- to stream Main, to step Merge: 000996
- to stream Main, to step Curation: 000995
Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">N‐Acyliminium Ion Chemistry: Highly Efficient and Versatile Carbon–Carbon Bond Formation by Nucleophilic Substitution of Hydroxy Groups Catalyzed by Sn(NTf2)4</title><author><name sortKey="Ben Thman, Raja" sort="Ben Thman, Raja" uniqKey="Ben Thman R" first="Raja" last="Ben Thman">Raja Ben Thman</name></author><author><name sortKey="Affani, Radouane" sort="Affani, Radouane" uniqKey="Affani R" first="Radouane" last="Affani">Radouane Affani</name></author><author><name sortKey="Tranchant, Marie Ose" sort="Tranchant, Marie Ose" uniqKey="Tranchant M" first="Marie-José" last="Tranchant">Marie-José Tranchant</name></author><author><name sortKey="Antoniotti, Sylvain" sort="Antoniotti, Sylvain" uniqKey="Antoniotti S" first="Sylvain" last="Antoniotti">Sylvain Antoniotti</name></author><author><name sortKey="Dalla, Vincent" sort="Dalla, Vincent" uniqKey="Dalla V" first="Vincent" last="Dalla">Vincent Dalla</name></author><author><name sortKey="Du Ach, Elisabet" sort="Du Ach, Elisabet" uniqKey="Du Ach E" first="Elisabet" last="Du Ach">Elisabet Du Ach</name></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:151E69B6A972D1B8DBF70EBBCAE3C16588E23AF5</idno><date when="2010" year="2010">2010</date><idno type="doi">10.1002/ange.200906036</idno><idno type="url">https://api.istex.fr/document/151E69B6A972D1B8DBF70EBBCAE3C16588E23AF5/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">000479</idno><idno type="wicri:Area/Istex/Curation">000479</idno><idno type="wicri:Area/Istex/Checkpoint">000179</idno><idno type="wicri:doubleKey">0044-8249:2010:Ben Thman R:n:acyliminium:ion</idno><idno type="wicri:Area/Main/Merge">000996</idno><idno type="wicri:Area/Main/Curation">000995</idno><idno type="wicri:Area/Main/Exploration">000995</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">N‐Acyliminium Ion Chemistry: Highly Efficient and Versatile Carbon–Carbon Bond Formation by Nucleophilic Substitution of Hydroxy Groups Catalyzed by Sn(NTf2)4</title><author><name sortKey="Ben Thman, Raja" sort="Ben Thman, Raja" uniqKey="Ben Thman R" first="Raja" last="Ben Thman">Raja Ben Thman</name><affiliation></affiliation><affiliation wicri:level="1"><country xml:lang="fr">Tunisie</country><wicri:regionArea>Present address: Unité de recherche en Matériaux, Energie et Environnement (MEE), Université de Gafsa, Sidi Ahmed Zarrouk, Gafsa</wicri:regionArea><wicri:noRegion>Gafsa</wicri:noRegion></affiliation></author><author><name sortKey="Affani, Radouane" sort="Affani, Radouane" uniqKey="Affani R" first="Radouane" last="Affani">Radouane Affani</name><affiliation><wicri:noCountry code="subField">(+33) 2‐3274‐4391</wicri:noCountry></affiliation></author><author><name sortKey="Tranchant, Marie Ose" sort="Tranchant, Marie Ose" uniqKey="Tranchant M" first="Marie-José" last="Tranchant">Marie-José Tranchant</name><affiliation><wicri:noCountry code="subField">(+33) 2‐3274‐4391</wicri:noCountry></affiliation></author><author><name sortKey="Antoniotti, Sylvain" sort="Antoniotti, Sylvain" uniqKey="Antoniotti S" first="Sylvain" last="Antoniotti">Sylvain Antoniotti</name><affiliation><wicri:noCountry code="subField">(+33) 4‐9207‐6125</wicri:noCountry></affiliation></author><author><name sortKey="Dalla, Vincent" sort="Dalla, Vincent" uniqKey="Dalla V" first="Vincent" last="Dalla">Vincent Dalla</name><affiliation></affiliation><affiliation wicri:level="1"><country wicri:rule="url">France</country></affiliation></author><author><name sortKey="Du Ach, Elisabet" sort="Du Ach, Elisabet" uniqKey="Du Ach E" first="Elisabet" last="Du Ach">Elisabet Du Ach</name><affiliation></affiliation><affiliation wicri:level="1"><country wicri:rule="url">France</country></affiliation></author></analytic><monogr></monogr><series><title level="j">Angewandte Chemie</title><title level="j" type="abbrev">Angewandte Chemie</title><idno type="ISSN">0044-8249</idno><idno type="eISSN">1521-3757</idno><imprint><publisher>WILEY‐VCH Verlag</publisher><pubPlace>Weinheim</pubPlace><date type="published" when="2010-01-18">2010-01-18</date><biblScope unit="volume">122</biblScope><biblScope unit="issue">4</biblScope><biblScope unit="page" from="788">788</biblScope><biblScope unit="page" to="792">792</biblScope></imprint><idno type="ISSN">0044-8249</idno></series><idno type="istex">151E69B6A972D1B8DBF70EBBCAE3C16588E23AF5</idno><idno type="DOI">10.1002/ange.200906036</idno><idno type="ArticleID">ANGE200906036</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0044-8249</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acetale</term><term>Katalyse</term><term>Lewis‐Säuren</term><term>N‐Acyliminium‐Ionen</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract">Atomökonomisch: Nichtmodifizierte N,O‐Halbacetale wurden in einer katalytischen, hocheffizienten α‐Amidoalkylierung kohlenstoffzentrierter Nucleophile eingesetzt, darunter Siliciumverbindungen, aktive Methylenderivate, elektronenreiche Arene und selbst einfache Ketone (siehe Schema). In der Regel genügt 1 Mol‐% des supersauren Lewis‐Reagens Sn(NTf2)4 als Katalysator.</div></front></TEI><affiliations><list><country><li>France</li><li>Tunisie</li></country></list><tree><noCountry><name sortKey="Affani, Radouane" sort="Affani, Radouane" uniqKey="Affani R" first="Radouane" last="Affani">Radouane Affani</name><name sortKey="Antoniotti, Sylvain" sort="Antoniotti, Sylvain" uniqKey="Antoniotti S" first="Sylvain" last="Antoniotti">Sylvain Antoniotti</name><name sortKey="Tranchant, Marie Ose" sort="Tranchant, Marie Ose" uniqKey="Tranchant M" first="Marie-José" last="Tranchant">Marie-José Tranchant</name></noCountry><country name="Tunisie"><noRegion><name sortKey="Ben Thman, Raja" sort="Ben Thman, Raja" uniqKey="Ben Thman R" first="Raja" last="Ben Thman">Raja Ben Thman</name></noRegion></country><country name="France"><noRegion><name sortKey="Dalla, Vincent" sort="Dalla, Vincent" uniqKey="Dalla V" first="Vincent" last="Dalla">Vincent Dalla</name></noRegion><name sortKey="Du Ach, Elisabet" sort="Du Ach, Elisabet" uniqKey="Du Ach E" first="Elisabet" last="Du Ach">Elisabet Du Ach</name></country></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 000995 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000995 | 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:151E69B6A972D1B8DBF70EBBCAE3C16588E23AF5
|texte= N‐Acyliminium Ion Chemistry: Highly Efficient and Versatile Carbon–Carbon Bond Formation by Nucleophilic Substitution of Hydroxy Groups Catalyzed by Sn(NTf2)4
}}
| This area was generated with Dilib version V0.6.25. |  |