Synthesis of enantiomerically pure juvenile hormone II

doi:10.1016/0957-4166(94)80140-1

Tetrahedron: Asymmetry

Volume 5, Issue 7, July 1994, Pages 1139-1142

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Abstract

An efficient preparative method for the enantiomerically pure juvenile hormone II has been developed by applying the diastereoselective alkylation and carbonyl reduction of an optically pure β-keto sulfoxide as the key steps.

Enantiomerically pure JH II can be synthesized based on the diastereoselective alkylation and carbonyl reduction of an enantiomerically β-keto sulfoxide.

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Tetrahedron: Asymmetry

Synthesis of enantiomerically pure juvenile hormone II

Abstract

Tetrahedron

J. Org. Chem.

J. Chem. Soc.

J. Am. Chem. Soc.

Proc. Natl. Acad. Sci. USA

Experientia

Experientia

J. Chem. Soc.

Tetrahedron Lett.