Literature DB >> 16986927

Asymmetric synthesis of 3-hydroxy-pyrrolidines via tin-lithium exchange and cyclization.

Guido Christoph1, Christian Stratmann, Iain Coldham, Dieter Hoppe.   

Abstract

We report a method for the synthesis of chiral pyrrolidines using tin-lithium exchange and cyclization reactions. The precursors are formed readily from simple starting materials and undergo tin-lithium exchange by treatment with n-butyllithium. Subsequent intramolecular carbolithiation is stereoselective to give highly enantiomerically enriched pyrrolidines in excellent yields.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16986927     DOI: 10.1021/ol061615p

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


  1 in total

1.  Synthesis of enantioenriched alpha-(hydroxyalkyl)-tri-n-butylstannanes.

Authors:  Anyu He; John R Falck
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.