Literature DB >> 24123536

Enantiodivergent deprotonation/acylation of α-amino nitriles.

Michiko Sasaki1, Tomo Takegawa, Kunihiro Sakamoto, Yuri Kotomori, Yuko Otani, Tomohiko Ohwada, Masatoshi Kawahata, Kentaro Yamaguchi, Kei Takeda.   

Abstract

Back to 'base'ics: The title reaction of enantioenriched α-ureidonitriles was found to proceed in a highly enantiodivergent manner despite the intermediacy of stereolabile α-nitrile metallocarbanions. Enantiodivergence is dependent upon the base used. For the less basic hexamethyldisilazides (HMDS), deprotonation in which a metal (M) cation is precomplexed with an electrophile is proposed. LDA=lithium diisopropylamide.
Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  asymmetric synthesis; carbanions; cyanides; lithium; metalation

Mesh:

Substances:

Year:  2013        PMID: 24123536     DOI: 10.1002/anie.201306443

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Highly enantioselective metallation-substitution alpha to a chiral nitrile.

Authors:  Arghya Sadhukhan; Melanie C Hobbs; Anthony J H M Meijer; Iain Coldham
Journal:  Chem Sci       Date:  2016-10-25       Impact factor: 9.825

2.  Sultones and Sultines via a Julia-Kocienski Reaction of Epoxides.

Authors:  Geoffrey M T Smith; Paul M Burton; Christopher D Bray
Journal:  Angew Chem Int Ed Engl       Date:  2015-10-27       Impact factor: 15.336

  2 in total

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