Issue 19, 1995

Concise enantiocontrolled synthesis of the A-ring precursor of calcitriol from the chiral cyclohexadienone synthon

Abstract

A new and concise enantiocontrolled route to the A-ring precursor of calcitriol is developed by utilizing the chiral cyclohexane-2,5-dienone synthon.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 1951-1952

Concise enantiocontrolled synthesis of the A-ring precursor of calcitriol from the chiral cyclohexadienone synthon

T. Kamikubo and K. Ogasawara, J. Chem. Soc., Chem. Commun., 1995, 1951 DOI: 10.1039/C39950001951

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