Literature DB >> 15498019

Asymmetric synthesis of C-aliphatic homoallylic amines and biologically important cyclohexenylamine analogues.

Chi-Lik Ken Lee1, Hui Yvonne Ling, Teck-Peng Loh.   

Abstract

An efficient method for the asymmetric synthesis of C-aliphatic homoallylic amines with up to 94% yield and 80% de is reported. Ring-closing metathesis of several chiral homoallylic amines using the second-generation Grubbs catalyst provided easy access to a wide variety of cyclohexenylamines.

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Year:  2004        PMID: 15498019     DOI: 10.1021/jo048903o

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Design, synthesis, and applications of chiral N-2-phenyl-2-propyl sulfinyl imines for group-assisted purification (GAP) asymmetric synthesis.

Authors:  Suresh Pindi; Jianbin Wu; Guigen Li
Journal:  J Org Chem       Date:  2013-03-26       Impact factor: 4.354

2.  Asymmetric allylboration of acyl imines catalyzed by chiral diols.

Authors:  Sha Lou; Philip N Moquist; Scott E Schaus
Journal:  J Am Chem Soc       Date:  2007-11-17       Impact factor: 15.419

  2 in total

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