Literature DB >> 12197717

Kinetic resolution of atropisomeric amides.

Ramon Rios1, Ciril Jimeno, Patrick J Carroll, Patrick J Walsh.   

Abstract

We have demonstrated the feasibility of the kinetic resolution of atropisomeric amides using the commercially avaliable AD-mix. To our knowledge, this methodology represents the first catalytic kinetic resolution of such compounds. Relative rates of up to 32 have been found for the kinetic resolution processes. We have also determined the barriers to rotation and half-lives of some of these amides. The half-lives range from 7 to 135 h at room temperature.

Entities:  

Year:  2002        PMID: 12197717     DOI: 10.1021/ja026436r

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  3 in total

1.  Enantioselective synthesis of atropisomeric benzamides through peptide-catalyzed bromination.

Authors:  Kimberly T Barrett; Scott J Miller
Journal:  J Am Chem Soc       Date:  2013-02-14       Impact factor: 15.419

2.  Engineered non-covalent π interactions as key elements for chiral recognition.

Authors:  Ming Yu Jin; Qianqian Zhen; Dengmengfei Xiao; Guanyu Tao; Xiangyou Xing; Peiyuan Yu; Chen Xu
Journal:  Nat Commun       Date:  2022-06-07       Impact factor: 17.694

3.  Proton donor acidity controls selectivity in nonaromatic nitrogen heterocycle synthesis.

Authors:  Simon Duttwyler; Shuming Chen; Michael K Takase; Kenneth B Wiberg; Robert G Bergman; Jonathan A Ellman
Journal:  Science       Date:  2013-02-08       Impact factor: 47.728

  3 in total

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