Literature DB >> 20302360

A straightforward three-component synthesis of alpha-amino esters containing a phenylalanine or a phenylglycine scaffold.

Caroline Haurena1, Erwan Le Gall, Stéphane Sengmany, Thierry Martens, Michel Troupel.   

Abstract

A range of alpha-amino esters has been synthesized in good to high yields using a straightforward three-component reaction among preformed or in situ generated aromatic or benzylic organozinc reagents, primary or secondary amines, and ethyl glyoxylate. The procedure, which is characterized by its simplicity, allows the concise synthesis of esters bearing a phenylglycine or a phenylalanine scaffold.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20302360     DOI: 10.1021/jo1002328

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


  3 in total

1.  A new manganese-mediated, cobalt-catalyzed three-component synthesis of (diarylmethyl)sulfonamides.

Authors:  Antoine Pignon; Erwan Le Gall; Thierry Martens
Journal:  Beilstein J Org Chem       Date:  2014-02-17       Impact factor: 2.883

2.  2-chlorophenyl zinc bromide: a convenient nucleophile for the mannich-related multicomponent synthesis of clopidogrel and ticlopidine.

Authors:  Isabelle Aillaud; Caroline Haurena; Erwan Le Gall; Thierry Martens; Gino Ricci
Journal:  Molecules       Date:  2010-11-11       Impact factor: 4.411

3.  Preparation of α-amino acids via Ni-catalyzed reductive vinylation and arylation of α-pivaloyloxy glycine.

Authors:  Xianghua Tao; Yanchi Chen; Jiandong Guo; Xiaotai Wang; Hegui Gong
Journal:  Chem Sci       Date:  2020-10-27       Impact factor: 9.825

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.