Issue 12, 1989

Control of angular methyl stereochemistry in diterpenoid synthetic intermediates

Abstract

The syn or anti disposition of the angular methyl groups in the tricycles (13) and (16) produced by divinylketene cyclisation is controlled by the stereochemistry of the vicinal substituent.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 784-786

Control of angular methyl stereochemistry in diterpenoid synthetic intermediates

L. Larsen and J. K. Sutherland, J. Chem. Soc., Chem. Commun., 1989, 784 DOI: 10.1039/C39890000784

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