Issue 17, 1992

Stereocontrolled synthesis of calyculin A: construction of the C(1)–C(14) tetraene nitrile unit

Abstract

An enantioselective and geometrically selective synthesis of the C(1)–C(14) tetraene nitrile unit of calyculin A, using aldol chemistry with (+)-(E)-diisopinocampheylborane and Stille coupling, is described.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1992, 1238-1240

Stereocontrolled synthesis of calyculin A: construction of the C(1)–C(14) tetraene nitrile unit

A. G. M. Barrett, J. J. Edmunds, J. A. Hendrix, K. Horita and C. J. Parkinson, J. Chem. Soc., Chem. Commun., 1992, 1238 DOI: 10.1039/C39920001238

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