
Bulletin of the Chemical Society of Japan p. 287 - 289 (1994)
Update date:2022-09-26
Topics:
Kunai, Atsutaka
Ueda, Takafumi
Toyoda, Eiji
Ishikawa, Mitsuo
Electrolytic reduction of dichloromethylphenyl-, dichlorodiphenyl-, dichloro-o-tolyl-, and dichlorodi-p-tolylsilanes in the presence of 2,3-dimethylbutadiene afforded 1-methyl-1-phenyl-, 1,1-diphenyl-, 1,1-di-o-tolyl-, and 1,1-di-p-tolyl-3,4-dimethyl-1-silacyclopent-3-ene, respectively, while the similar reaction of chloromethyldiphenylsilane with 2,3-dimethylbutadiene afforded 1-(methyldiphenylsilyl)- and 1,4-bis(methyldiphenylsilyl)-2,3-dimethyl-2-butene.A reaction mechanism leading to these products has been discussed.
View MoreContact:+86-371-55981030
Address:Room 1571, Macalline Soho, No.1, Shangdu Road, Zhengzhou, Henan
Shanghai united Scientific Co.,Ltd.
Contact:+86-21-53535353
Address:28F No.900 huaihai Road Shanghai China
Dalian RSD International Trade Co.,Ltd.(expird)
Contact:86-22-60875058 58610575
Address:Wantong International Areas, Hongqiao District, Tianjin, China.China
Contact:+86-571-86491666
Address:SHI XIANG ROAD
Taizhou volsen chemical Co., Ltd
website:http://www.volsenchem.com
Contact:+86-576-88869393
Address:Jiaojiang District, Taizhou, Zhejiang, China.
Doi:10.1016/S0040-4020(01)96947-9
(1965)Doi:10.1002/jhet.5570120143
(1975)Doi:10.1021/ja01556a079
()Doi:10.1021/j100885a045
()Doi:10.1002/anie.201907572
(2019)Doi:10.1007/s11224-016-0809-7
(2016)