Issue 16, 1990

A long-range intramolecular functionalization by alkoxyl radicals: a long-range intramolecular oxygenation of C(15) of the androstane skeleton

Abstract

The first example of a one-step introduction of a carbonyl group to C(15) of the 5α-androstane skeletion, based on a long-range intramolecular hydrogen abstraction by alkoxyl radicals, generated by irradiation of 5α-androstane esters carrying a benzhydryl group in carbon tetrachloride containing mercury(II) oxide and iodine, is described.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 1074-1076

A long-range intramolecular functionalization by alkoxyl radicals: a long-range intramolecular oxygenation of C(15) of the androstane skeleton

K. Orito, M. Ohto and H. Suginome, J. Chem. Soc., Chem. Commun., 1990, 1074 DOI: 10.1039/C39900001074

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