Opening of steroid ring a by means of lead tetraacetate

Abstract

The lead tetraacetate oxidation of cholestan-1β-ol and cholestan-1α-ol in benzene solution did not afford cyclic ethers but resulted, in major part, in the opening of ring A with formation of 1,10-seco-aldehydes. In addition, cholestane, cholest-1-ene and cholestan-1-one were also obtained

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Last time updated on 24/05/2021

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