Journal article
Pd-Catalyzed alpha-Arylation of Nitriles and Esters and gamma-Arylation of Unsaturated Nitriles with TMPZnCl center dot LiCl
Organic letters, v 13(7), pp 1690-1693
01 Apr 2011
PMID: 21366325
Abstract
Using TMPZnCl center dot"LiCl as a kinetically highly active base, nitriles and esters undergo a Pd-catalyzed alpha-arylation under mild conditions. Remarkably, in the case of alpha,beta or beta,gamma-unsaturated nitriles, a regioselective gamma-arylation or a gamma-alkenylation is observed.
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Details
- Title
- Pd-Catalyzed alpha-Arylation of Nitriles and Esters and gamma-Arylation of Unsaturated Nitriles with TMPZnCl center dot LiCl
- Creators
- Stephanie Duez - Duquesne UniversitySebastian Bernhardt - Duquesne UniversityJohannes Heppekausen - Duquesne UniversityFraser F. Fleming - Duquesne UniversityPaul Knocher - Ludwig Maximilian University of Munich
- Publication Details
- Organic letters, v 13(7), pp 1690-1693
- Publisher
- American Chemical Society; Washington, DC
- Number of pages
- 4
- Grant note
- Fonds der Chemischen Industrie European Research Council (ERC); European Commission; Spanish Government Center of Advanced Studies, Ludwig Maximilians-Universitat Munchen (CAS); Chinese Academy of Sciences Deutsche Forschungsgemeinschaft (DFG); German Research Foundation (DFG)
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- Chemistry
- Web of Science ID
- WOS:000288691600029
- Scopus ID
- 2-s2.0-79953182737
- Other Identifier
- 991020898498704721
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- Collaboration types
- Domestic collaboration
- International collaboration
- Web of Science research areas
- Chemistry, Organic