Literature DB >> 21952931

Enantioselective synthesis of α-deuterium labelled chiral α-amino acids via dynamic kinetic resolution of racemic azlactones.

Joong-Suk Oh1, Kyung Il Kim, Choong Eui Song.   

Abstract

Catalytic dynamic kinetic resolution (DKR) of racemic azlactones with EtOD using squaramide-based dimeric cinchona alkaloid organocatalysts is shown to be a highly effective strategy for the preparation of enantiomerically pure α-deuterated chiral α-amino acids.

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Year:  2011        PMID: 21952931     DOI: 10.1039/c1ob06319g

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

1.  Origin of and a Solution for Uneven Efficiency by Cinchona Alkaloid-Derived, Pseudoenantiomeric Catalysts for Asymmetric Reactions.

Authors:  Bin Hu; Mark W Bezpalko; Chao Fei; Diane A Dickie; Bruce M Foxman; Li Deng
Journal:  J Am Chem Soc       Date:  2018-10-09       Impact factor: 15.419

2.  Synthesis of Enantioenriched α-Deuterated α-Amino Acids Enabled by an Organophotocatalytic Radical Approach.

Authors:  Peng Ji; Yueteng Zhang; Yue Dong; He Huang; Yongyi Wei; Wei Wang
Journal:  Org Lett       Date:  2020-02-11       Impact factor: 6.005

3.  Catalytic asymmetric synthesis of enantioenriched α-deuterated pyrrolidine derivatives.

Authors:  Xin Chang; Xiang Cheng; Chun-Jiang Wang
Journal:  Chem Sci       Date:  2022-03-17       Impact factor: 9.825

  3 in total

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