An enantioselective chemoenzymatic synthesis of the four 1-amino 2-methylcyclopropane carboxylic acids

Article abstract of DOI:10.1080/00397919208021100

Racemic 2-methylcyclopropane dicarboxylic acid dimethyl ester undergoes selective enzymatic reactions to give enantiomerically pure monocarboxylic acids which by classical organic chemistry lead to the four 1-amino 2-methyl cyclproane carboxylic acids.

Full text of DOI:10.1080/00397919208021100

Synthetic Communications
ISSN: 0039-7911 (Print) 1532-2432 (Online) Journal homepage: http://www.tandfonline.com/loi/lsyc20
An Enantioselective Chemoenzymatic Synthesis
of the Four 1-Amino 2-Methylcyclopropane
Carboxylic Acids
F. Rusconi di Lugano , J. Monteiro , C. Fliche , J. Braun & F. Le Goffic
To cite this article: F. Rusconi di Lugano , J. Monteiro , C. Fliche , J. Braun & F. Le
Goffic (1992) An Enantioselective Chemoenzymatic Synthesis of the Four 1-Amino 2-
Methylcyclopropane Carboxylic Acids, Synthetic Communications, 22:8, 1155-1158, DOI:
10.1080/00397919208021100
To link to this article: http://dx.doi.org/10.1080/00397919208021100
Published online: 23 Sep 2006.
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Date: 22 June 2016, At: 17:50