Issue 21, 1996
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Chemoenzymatic routes to chiral (non-racemic) cyclopropanes. Preparation of a key intermediate for the synthesis of (1R)-cis-pyrethroids

Martin G. Banwell  and  Grant S. Forman  

Abstract

The microbial oxidation product 2 (X = Br) has been converted into the chiral (non-racemic) cyclopropane 11, a synthon for the commercially significant (1R)-cis-pyrethroid class of insecticides.

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Article information

DOI
https://doi.org/10.1039/P19960002565
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1996, 2565-2566

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Chemoenzymatic routes to chiral (non-racemic) cyclopropanes. Preparation of a key intermediate for the synthesis of (1R)-cis-pyrethroids

M. G. Banwell and G. S. Forman, J. Chem. Soc., Perkin Trans. 1, 1996, 2565 DOI: 10.1039/P19960002565

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