Australian Journal of Chemistry p. 701 - 710 (1988)
Update date:2022-09-26
Topics:
Burgess, Vicky A.
Easton, Christopher J.
Hay, Michael P.
Steel, Peter J.
The bromide (5), prepared by treatment of the glycine derivative (4) with N-bromosuccinimide, reacted with hexabutylditin to give diastereoisomers of the glycine dimer (7), only when moisture was rigorously excluded from the reaction.Otherwise the major products were the diastereoisomers of the ether (11).The structure of the racemic diastereoisomer (11) was determined by X-ray crystallography.Photolysis of mixtures of the glycine derivative (4) and di-t-butyl peroxide gave the alanine derivative (10) in addition to the diastereoisomeric dimers (7).
View MoreSuzhou Tianma Specialty Chemicals Co.,Ltd
Contact:+86-512-68090577
Address:#199, Huayuan Rd, Mudu, Suzhou, Jiangsu, CHINA
Xi'an yuanfar international trade company
website:https://www.yuanfarchemical.com
Contact:86-029-88745613 ext 828
Address:Floor19th ,B Building, Oak Block,No.36 South Fenghui Road, Dev. Zone of High-Tech Ind.,Xi’an, China
Lanzhou huibang biological chemical technology Co., LTD
Contact:0931-7843964
Address:NO.2011,Yannan Road,Chengguan,
Wuhan Sunrise Pharmaceutical Technology Co., Ltd
Contact:+86-27-83314682
Address:Room 340, New material Industrial base No.17, Gu Tian Five Lu , Qiaokou District, Wuhan , China
Shanghai Bojing Chemical Co., Ltd.
Contact:021-37122233
Address:6F Buildiing 11,No.388,Baifu Road,District Fengxian.Shanghai, China.
Doi:10.1021/jm300735t
(2012)Doi:10.1002/jhet.1857
(2014)Doi:10.1016/S0031-9422(97)00024-1
(1997)Doi:10.1039/b908447a
(2009)Doi:10.1016/j.ejmech.2009.06.001
(2009)Doi:10.1016/j.tetlet.2014.09.089
(2014)
