Journal of Organometallic Chemistry p. 173 - 181 (1990)
Update date:2022-08-02
Topics:
Weidenbruch, Manfred
Schaefers, Karen
Peters, Karl
Schnering, Hans Georg von
Treatment of di-t-butyldichlorostannane with sterically congested aryllithium compounds gives di-t-butylchloro(mesityl)stannane (2) and di-t-butylchloro(2,4,6-tri-t-butylphenyl)stannane (3), both of which show restricted rotation about the Sn-C(Ar) bond at room temperature.Reductive chloride elimination from 2 yields the corresponding distannane, whereas a similar reaction of 3 only results in decomposition.Reaction of 3 with t-butyllithium by hydrogen abstraction from one of the ortho-t-butylmethyl groups gives the stannaindane derivative (6).The structures of 3 and 6 have been confirmed by X-ray crystallography.
View MoreHangzhou Deli Chemical Co.,Ltd.
website:http://www.dlchemical.com
Contact:86 571 28006267
Address:Tangxi Industrial Area, Yuhang District, Hangzhou
Hangzhou Taiyan Trading Co., Ltd(expird)
Contact:+86-13777583958
Address:NO.63, Xingyi Street, Xihu District, Hangzhou, Zhejiang, China
Anhui Gusheng Import&Export CO.,LTD
Contact:86-551-63662296
Address:Jinzhai Road NO.162 ,hefei, china
Sanming Coffer Fine Chemical Industrial Co., Ltd
website:http://www.cofferxm.com/
Contact:+86-598-5853979
Address:Jin-sha Yuan Chuang-ye Park,Hi-Tech Development Zone,Sanming City P.R.China
Zhejiang Golden-Shell Pharmaceutical Co.,Ltd.
Contact:+86-576-87501888 / 87501988
Address:No.89 Zhongxing Road. Li'ao, Yuhuan, Zhejiang, China
Doi:10.1007/BF01168106
(1989)Doi:10.1007/s00726-010-0651-y
(2011)Doi:10.1134/S107042721012013X
(2010)Doi:10.1021/jo00299a020
(1990)Doi:10.1016/S0040-4020(01)89222-X
(1989)Doi:10.1016/j.poly.2019.02.027
(2019)