Concise Enantiocontrolled Synthesis of the A-Ring Precursor of Calcitriol from the Chiral Cyclohexadienone Synthon

DOI: 10.1039/c39950001951

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1951 - 1952 (1995)

Update date:2022-08-15

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Authors:

Kamikubo, Takashi

Ogasawara, Kunio

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Article abstract of DOI:10.1039/c39950001951

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

Full text of DOI:10.1039/c39950001951

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