Journal of the Chemical Society. Chemical communications p. 119 - 120 (1993)
Update date:2022-08-18
Topics:
Fouche, Gerda
Horak, R. Martinus
Meth-Cohn, Otto
3-Phenyl-2,3-epoxy ketones are transformed using baker's yeast into the corresponding 1,2,3-triols as one pure diastereoisomer (S,S,S and R,R,R) formed by syn ring opening of the epoxide after first reduction of the carbonyl group; the reaction results in the epoxy-oxygen becoming the mid OH group of the triol, implicating enzyme attack at the C-3 in the ring-opening reaction.
View MoreContact:852-27701081
Address:Room 2509, New Tech Plaza, 34 Tai Yau St., San Po Kong, HK
Beijing Tianjia Chemical Science & Technology Co.,Ltd
Contact:86-0550-2392698
Address:No.388, Shiliang Road (East),
Mollt Biochem Co., Ltd(expird)
Contact:+86-21-38682181
Address:shanghai ,china
Chengdu Baishixing Science and Technology Industry Co., Ltd.
website:http://www.cd-bsx.com
Contact:+86-28-88531548
Address:#217,North of Industry Road,Heshan Town,Pujiang County,Chengdu,Sichuan,China.
website:http://www.orchid-chem.com
Contact:+86-571-85395792
Address:607, North Zhongshan Road, Hangzhou 310000 China
Doi:10.1080/10587259508038694
(1995)Doi:10.1039/c39870000825
(1987)Doi:10.1021/acs.joc.9b00495
(2019)Doi:10.1016/j.bmcl.2010.08.084
(2010)Doi:10.1007/s11095-013-0976-9
(2013)Doi:10.1021/jo00249a004
(1988)
