| Literature DB >> 29617139 |
Kazuhiro Matsumoto1, Jiadi Huang1, Yuki Naganawa1, Haiqing Guo1, Teruo Beppu1, Kazuhiko Sato1, Shigeru Shimada1, Yumiko Nakajima1.
Abstract
A nickel complex/Lewis acid combination effectively catalyzed the direct silyl-Heck reaction of chlorosilanes, which are key raw materials in the organosilicon industry, to give synthetically important alkenylsilane products. Trichlorosilanes, dichlorosilanes, and monochlorosilanes underwent the silyl-Heck reaction to afford the corresponding alkenylsilanes in high yields. In the reactions of dichlorosilanes, a single substitution occurred to give monoalkenylsilanes in a highly selective manner.Entities:
Year: 2018 PMID: 29617139 DOI: 10.1021/acs.orglett.8b00847
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005