Issue 16, 1997
From the journal:

Chemical Communications

Unusual generation of methoxy groups in Barton deoxygenations of alcohols

Caroline S. Bensasson,   Sir John Cornforth,   Ming-Hui Du  and  James R. Hanson  

Abstract

Reaction of the S-methyl dithiocarbonate of lanosterol with excess of tributyltin deuteride and azoisobutyronitrile in benzene afforded lanosteryl methyl ether in which all hydrogen in the methoxy group originated from the organotin reagent.

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Article information

DOI
https://doi.org/10.1039/A703156D
Article type
Paper

Chem. Commun., 1997, 1509-1510

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Unusual generation of methoxy groups in Barton deoxygenations of alcohols

C. S. Bensasson, S. John Cornforth, M. Du and J. R. Hanson, Chem. Commun., 1997, 1509 DOI: 10.1039/A703156D

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