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 MoreContact:86-21 60347964
Address:No.1304, West Meilong Road, Minhang District, Shanghai, China
Contact:86-931-8272767
Address:Room 602, No.461, Nanchang Road, Chengguan District, Lanzhou City, China PRC
Anhui Xinyuan Technology Co.,Ltd
Contact:0086-559-3515800
Address:No.16 Zijin Rd, Circular Economic Zone, Huizhou District, Huangshan Anhui China
Contact:+49-4101-3053-0
Address:Waldhofstrasse 14 ,25474 Ellerbek Germany
Contact:+44 (0)161 367 9441
Address:
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)
