Literature DB >> 19146452

Asymmetric Lewis acid mediated [1,2]-rearrangement of proline-derived ammonium ylides.

Pavel Tuzina1, Peter Somfai.   

Abstract

The first example of asymmetric Lewis acid mediated [1,2]-rearrangement of N-benzylic proline amides to form quaternary proline derivatives is reported. The presented reaction is shown to proceed with remarkable high C-->N-->C chirality transfer. Various quaternary proline derivatives have been prepared in good to excellent yields and high enantiomeric purity.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19146452     DOI: 10.1021/ol8028803

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


  2 in total

1.  Competitive [2,3]- and [1,2]-oxonium ylide rearrangements. Concerted or stepwise?

Authors:  Deana M Jaber; Ryan N Burgin; Matthew Helper; Peter Y Zavalij; Michael P Doyle
Journal:  Org Lett       Date:  2012-03-12       Impact factor: 6.005

2.  Enantioselective synthesis of Iboga alkaloids and vinblastine via rearrangements of quaternary ammoniums.

Authors:  Yun Zhang; Yibin Xue; Gang Li; Haosen Yuan; Tuoping Luo
Journal:  Chem Sci       Date:  2016-05-16       Impact factor: 9.825

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.