[reaction: see text] When carbonyl compounds were allowed to react with phenyl trimethylsilyl selenide and tributylstannyl hydride in the presence of a catalytic amount of AIBN as a radical initiator, the hydrosilylation of the carbonyl compounds efficiently proceeded to give the corresponding silyl ethers in moderate to good yields.
No takes yet. Share an insight, caveat, or question.
Nishiyama et al. (2001) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: