365413-70-3Relevant academic research and scientific papers
Tin-free radical acylation reactions with methanesulfonyl oxime ether
Kim, Sunggak,Song, Hyun-Ji,Choi, Tae-Lim,Yoon, Joo-Yong
, p. 2524 - 2526 (2001)
A simple strategy involving thermal decomposition of the methanesulfonyl radical into the methyl radical and the subsequent transfer of an iodine atom or phenyl telluride group was used to develop a tin-free radical acylation reaction (see scheme; V-40 = 1,1′-azobis(cyclohexane-1-carbonitrile). The key was finding reaction conditions under which the I or PhTe transfer is faster than the direct addition of the alkyl radical to the methanesulfonyl ether.
