Journal of the Chemical Society. Chemical communications p. 1018 - 1019 (1986)
Update date:2022-08-16
Topics:
Soai, Kenso
Niwa, Seiji
Yamanoi, Takashi
Hikima, Hitoshi
Ishizaki, Miyuki
Optically active 2-aryl substituted oxetanes are synthesised in high enantiomeric excesses (up to 89percent e.e.) via enantioselective reduction of β-halogenoketones with lithium borohydride using (R,R')-N,N'-dibenzoylcystine and t-butyl alcohols as ligands.
View MoreContact:86-021-52418058
Address:8/F, Building 6, Guiping Road No.333, Shanghai, 200233, China
Tianjin Pharmacn Medical Technology Co.,Ltd.
Contact:86-22-60122566ext.866(English),23359620
Address:Green Industrial Base, 6 Haitaifazhan Sixth Rd., Huayuan Industrial Area, Tianjin, 300384, China
Taizhou Elitechemie MediPharma Technology Co.,Ltd.
Contact:+86-523-86810021
Address:Building G14,NO.1 Avenue,China Medical City, Taizhou, Jiangsu,China
SHANXI XINTIANYUAN PHARMACEUTICAL CO., LTD.
website:http://www.tychemical.com
Contact:0086-358-3521713 3521715
Address:No. 1 Yintong Road, Shanxi Jiaocheng Economic Development Zone, Xiajiaying Town, Jiaocheng County, Lvliang City, Shanxi Province, China
Hangzhou Haiqiang Chemical Co.,Ltd.
Contact:+86-571-86960370
Address:Add: 5/F, Around Town North Road,No. 10, Hangzhou, Zhejiang,China
Doi:10.1021/jo01050a043
(1962)Doi:10.1016/j.dyepig.2018.04.052
(2018)Doi:10.1016/j.jcat.2003.08.008
(2004)Doi:10.1021/acs.joc.0c02246
(2020)Doi:10.1002/cbic.201700071
(2017)Doi:10.1016/S0040-4039(97)00948-9
(1997)
