
Journal of Organometallic Chemistry p. 137 - 146 (1982)
Update date:2022-08-02
Topics:
Castel, A.
Riviere, P.
Satge, J.
Catalytic activity of nuclophiles such as tertiary amines and diazo derivatives in the reduction of halogermanes by means of gentle reductive agents, such as R3M(IVB)-H or RCHO, has been shown.In the particular case of enolisable aldehyde, a competition between nucleophilic substitution at the metal and germanium-halogen bond reduction has been observed.Transposition of enoxygermanes formed through the substitution process, leads to β-germylaldehydes.
website:http://www.simagchem.com
Contact:+86-592-2680277
Address:21/F Hualong Office Building,No.6 Hubin East Road, Xiamen,China
Beijing Apis Biotechnology Co., Ltd.
Contact:86-010-67856775-8551
Address:NO.4PUHUANGYU ROAD,FENTAI DISTRICT, BEIJING, CHINA
Beyond Pharmaceutical Co., Ltd
Contact:+86-571-8195-3185
Address:No. 13-1, Liansheng Road, Yuhang District
Feis International Trade Co,. Ltd
Contact:13961823444-18235944442
Address:Wuxi jiangsu
Hangzhou Ledun Technology Co.,Ltd.
Contact:86-571-18767088918
Address:No.6 street,XiaSha,Hangzhou,China.
Doi:10.1002/jlcr.3885
(2021)Doi:10.1021/ja00340a021
(1983)Doi:10.1016/0022-328X(91)86228-I
(1991)Doi:10.1016/j.bmcl.2007.04.024
(2007)Doi:10.1039/P19820002391
(1982)Doi:10.1002/jps.2600710922
(1982)