Issue 19, 1995

A facile stereoselective route to a C/D-ring synthon for 20-epi-22-oxavitamin D3 analogues

Abstract

An efficient method for the preparation of a C/D-ring synthon for 20-epi-22-oxavitamin D3 analogues is developed based on Me3SiOSO2CF3 catalysed reductive etherification of a ketone with an alkoxytrimethylsilane in the presence of triethylsilane.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 1959-1960

A facile stereoselective route to a C/D-ring synthon for 20-epi-22-oxavitamin D3 analogues

S. Hatakeyama, T. Ikeda, H. Irie, C. Izumi, H. Mori, K. Uenoyama, H. Yamada and M. Nishizawa, J. Chem. Soc., Chem. Commun., 1995, 1959 DOI: 10.1039/C39950001959

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