[GRAPHICS] 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.
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Hokkaido Univ, Organ Synth Lab, Div Mol Chem, Grad Sch Engn, Sapporo, Hokkaido 0608628, JapanHokkaido Univ, Organ Synth Lab, Div Mol Chem, Grad Sch Engn, Sapporo, Hokkaido 0608628, Japan
Orito, K
Uchiito, S
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Hokkaido Univ, Organ Synth Lab, Div Mol Chem, Grad Sch Engn, Sapporo, Hokkaido 0608628, JapanHokkaido Univ, Organ Synth Lab, Div Mol Chem, Grad Sch Engn, Sapporo, Hokkaido 0608628, Japan
Uchiito, S
Satoh, Y
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Hokkaido Univ, Organ Synth Lab, Div Mol Chem, Grad Sch Engn, Sapporo, Hokkaido 0608628, JapanHokkaido Univ, Organ Synth Lab, Div Mol Chem, Grad Sch Engn, Sapporo, Hokkaido 0608628, Japan
Satoh, Y
Tatsuzawa, T
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Hokkaido Univ, Organ Synth Lab, Div Mol Chem, Grad Sch Engn, Sapporo, Hokkaido 0608628, JapanHokkaido Univ, Organ Synth Lab, Div Mol Chem, Grad Sch Engn, Sapporo, Hokkaido 0608628, Japan
Tatsuzawa, T
Harada, R
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Hokkaido Univ, Organ Synth Lab, Div Mol Chem, Grad Sch Engn, Sapporo, Hokkaido 0608628, JapanHokkaido Univ, Organ Synth Lab, Div Mol Chem, Grad Sch Engn, Sapporo, Hokkaido 0608628, Japan
Harada, R
Tokuda, M
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Hokkaido Univ, Organ Synth Lab, Div Mol Chem, Grad Sch Engn, Sapporo, Hokkaido 0608628, JapanHokkaido Univ, Organ Synth Lab, Div Mol Chem, Grad Sch Engn, Sapporo, Hokkaido 0608628, Japan