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Verkade's Superbase as an Organocatalyst for the Strecker Reaction

Authors :
Yang, Jian
Chatelet, Bastien
Ziarelli, Fabio
Dufaud, Véronique
hérault, damien
Martinez, Alexandre
Institut des Sciences Moléculaires de Marseille (ISM2)
Aix Marseille Université (AMU)-École Centrale de Marseille (ECM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Spectropôle - Aix Marseille Université (AMU SPEC)
Centre National de la Recherche Scientifique (CNRS)-Aix Marseille Université (AMU)
Laboratoire de Chimie, Catalyse, Polymères et Procédés, R 5265 (C2P2)
Université Claude Bernard Lyon 1 (UCBL)
Université de Lyon-Université de Lyon-École supérieure de Chimie Physique Electronique de Lyon (CPE)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)
Université de Lyon-Université de Lyon-École Supérieure de Chimie Physique Électronique de Lyon (CPE)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Nanjing University of Science and Technology [Nanjing]
Centre National de la Recherche Scientifique (CNRS)-École Centrale de Marseille (ECM)-Aix Marseille Université (AMU)
Source :
European Journal of Organic Chemistry, European Journal of Organic Chemistry, Wiley-VCH Verlag, 2018, 2018 (45), pp.6328-6332. ⟨10.1002/ejoc.201801170⟩, European Journal of Organic Chemistry, 2018, 2018 (45), pp.6328-6332. ⟨10.1002/ejoc.201801170⟩
Publication Year :
2018
Publisher :
HAL CCSD, 2018.

Abstract

International audience; Proazaphosphatranes-Verkade's superbases-proved to be efficient organocatalysts for the Strecker reaction between protected imines and trimethylsilyl cyanide (TMSCN). Excellent to quantitative yields were reached and, compared to other systems, only low catalyst loading and short reaction times were required for the reaction to proceed efficiently. A remarkable initial turnover frequency (TOF), close to 105 h–1, was achieved, associated with an excellent selectivity since no side reactions were observed. A reaction mechanism was proposed and the key role played by the apical nitrogen in the proazaphosphatrane structure was demonstrated.

Details

Language :
English
ISSN :
1434193X and 10990690
Database :
OpenAIRE
Journal :
European Journal of Organic Chemistry, European Journal of Organic Chemistry, Wiley-VCH Verlag, 2018, 2018 (45), pp.6328-6332. ⟨10.1002/ejoc.201801170⟩, European Journal of Organic Chemistry, 2018, 2018 (45), pp.6328-6332. ⟨10.1002/ejoc.201801170⟩
Accession number :
edsair.dedup.wf.001..b27e8eb13286656739f7739a2a954210