Literature DB >> 21517112

Enantioselective α-amination of branched aldehydes promoted by simple chiral primary amino acids.

Ji-Ya Fu1, Qing-Chuan Yang, Qi-Lin Wang, Jun-Nan Ming, Fei-Ying Wang, Xiao-Ying Xu, Li-Xin Wang.   

Abstract

A series of simple chiral primary amino acids were first successfully applied to promote the enantioselective α-amination of branched aldehydes with azadicarboxylates and the desired adducts bearing quaternary stereogenic centers were obtained in excellent yields (up to 99%) and enantioselectivities (up to 97% ee).

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Year:  2011        PMID: 21517112     DOI: 10.1021/jo102361h

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


  2 in total

1.  Direct asymmetric amination of α-branched cyclic ketones catalyzed by a chiral phosphoric acid.

Authors:  Xiaoyu Yang; F Dean Toste
Journal:  J Am Chem Soc       Date:  2015-02-26       Impact factor: 15.419

2.  Asymmetric amination of α,α-dialkyl substituted aldehydes catalyzed by a simple chiral primary amino acid and its application to the preparation of a S1P1 agonist.

Authors:  Qiong Xiao; Yifan Tang; Ping Xie; Dali Yin
Journal:  RSC Adv       Date:  2019-10-18       Impact factor: 4.036

  2 in total

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