Journal of Organometallic Chemistry p. C48 - C50 (1981)
Update date:2022-09-26
Topics:
Ishikawa, Mitsuo
Nakagawa, Ken-Ichi
Katayama, Seiji
Kumada, Makoto
Photochemically generated trimethylsilylphenylsilylene reacted with octyl chloride and cyclopropylcarbinyl chloride to give the respective formal carbon-chlorine insertion products.With sec-butyl chloride, trimethylsilylphenylsilylene afforded both the carbon-chlorine insertion product and 1-chloro-1-phenyl-2,2,2-trimethyldisilane (IV), while with tert-butyl chloride, IV was obtained as the sole volatile product.
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Doi:10.1002/jps.2600700804
(1981)Doi:10.1016/0040-4039(94)02209-T
(1995)Doi:10.1016/S0022-328X(00)86630-9
(1981)Doi:10.1016/S0020-1693(00)83739-1
(1981)Doi:10.1021/ja046154m
(2004)Doi:10.1016/S0040-4039(01)90563-5
(1981)
