Literature DB >> 12762758

Highly enantioselective synthesis of alpha-alkyl-alanines via the catalytic phase-transfer alkylation of 2-naphthyl aldimine tert-butyl ester by using O(9)-allyl-N(1)-2',3',4'-trifluorobenzylhydrocinchonidinium bromide.

Sang-sup Jew1, Byeong-Seon Jeong, Jeong-Hee Lee, Mi-Sook Yoo, Yeon-Ju Lee, Boon-saeng Park, Myoung Goo Kim, Hyeung-geun Park.   

Abstract

Systematic investigations to develop an efficient enantioselective synthetic method for alpha-alkyl-alanine by catalytic phase-transfer alkylation were performed. The alkylation of 2-naphthyl aldimine tert-butyl ester, 1E, with RbOH and O(9)-allyl-N-2',3',4'-trifluorobenzylhydrocinchonidinium bromide, 6, at -35 degrees C showed the highest enantioselectivities, up to 96% ee.

Entities:  

Year:  2003        PMID: 12762758     DOI: 10.1021/jo034006t

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  4 in total

1.  Catalytic Enantioselective Electrophilic Aminations of Acyclic α-Alkyl β-Carbonyl Nucleophilies.

Authors:  Xiaofeng Liu; Bingfeng Sun; Li Deng
Journal:  Synlett       Date:  2009-06       Impact factor: 2.454

2.  Synthesis of quaternary α-methyl α-amino acids by asymmetric alkylation of pseudoephenamine alaninamide pivaldimine.

Authors:  Cedric L Hugelshofer; Kevin T Mellem; Andrew G Myers
Journal:  Org Lett       Date:  2013-06-07       Impact factor: 6.005

3.  Dimeric cinchona ammonium salts with benzophenone linkers: enantioselective phase transfer catalysts for the synthesis of α-amino acids.

Authors:  Seunga Woo; Yong-Gyun Kim; Baegeun Lim; Jiin Oh; Yeonji Lee; Hyeri Gwon; Keepyung Nahm
Journal:  RSC Adv       Date:  2018-01-09       Impact factor: 4.036

4.  Synthesis of Both Enantiomers of Chiral Phenylalanine Derivatives Catalyzed by Cinchona Alkaloid Quaternary Ammonium Salts as Asymmetric Phase Transfer Catalysts.

Authors:  Lei Jin; Shuai Zhao; Xin Chen
Journal:  Molecules       Date:  2018-06-12       Impact factor: 4.411

  4 in total

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