Literature DB >> 30916975

Asymmetric Synthesis of α-Amino Acids by Organocatalytic Biomimetic Transamination.

Qi-Kai Kang1, Sermadurai Selvakumar1, Keiji Maruoka1,2.   

Abstract

A biomimetic enantioselective transamination of α-keto ester derivatives can be realized under mild conditions by using chiral quaternary ammonium arenecarboxylates in the absence of base additives. The corresponding α-amino acids can be used as versatile intermediates for further synthetic transformations that furnish chiral pyrrolidine and octahydroindolizine derivatives.

Entities:  

Year:  2019        PMID: 30916975     DOI: 10.1021/acs.orglett.9b00588

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


  2 in total

1.  Comparison of mesoporous fractal characteristics of silica-supported organocatalysts derived from bipyridine-proline and resultant effects on the catalytic asymmetric aldol performances.

Authors:  Guangpeng Xu; Liujie Bing; Bingying Jia; Shiyang Bai; Jihong Sun
Journal:  RSC Adv       Date:  2022-04-07       Impact factor: 3.361

2.  New Mesoporous Silica-Supported Organocatalysts Based on (2S)-(1,2,4-Triazol-3-yl)-Proline: Efficient, Reusable, and Heterogeneous Catalysts for the Asymmetric Aldol Reaction.

Authors:  Omar Sánchez-Antonio; Kevin A Romero-Sedglach; Erika C Vázquez-Orta; Eusebio Juaristi
Journal:  Molecules       Date:  2020-10-03       Impact factor: 4.411

  2 in total

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