Literature DB >> 28406311

Organocatalytic Asymmetric Decarboxylative Amination of β-Keto Acids: Access to Optically Active α-Amino Ketones and 1,2-Amino Alcohols.

Yi Wei1, Heng-Xia Zhang1, Jun-Liang Zeng1, Jing Nie1, Jun-An Ma1.   

Abstract

An organocatalytic asymmetric decarboxylative amination reaction of β-keto acids is described. Under mild reaction conditions, a series of chiral α-amino ketones were obtained in good to high yields (up to 99%) and enantioselectivities (up to 95% ee). A chiral 1,2-amino alcohol was synthesized from the corresponding decarboxylative amination product in several steps without loss of enantioselectivity.

Entities:  

Year:  2017        PMID: 28406311     DOI: 10.1021/acs.orglett.7b00797

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Enantioselective amination of 4-alkylisoquinoline-1,3(2H,4H)-dione derivatives.

Authors:  Cheng Cheng; Ying-Xian Li; Xue-Min Jia; Ji-Quan Zhang; Yong-Long Zhao; Wei Feng; Lei Tang; Yuan-Yong Yang
Journal:  RSC Adv       Date:  2020-11-25       Impact factor: 4.036

2.  Direct catalytic enantioselective amination of ketones for the formation of tri- and tetrasubstituted stereocenters.

Authors:  B M Trost; J S Tracy; T Saget
Journal:  Chem Sci       Date:  2018-02-14       Impact factor: 9.825

  2 in total

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