
Helvetica Chimica Acta p. 638 - 644 (1992)
Update date:2022-08-05
Topics:
Erdmann, Peter
Schaefer, Joerg
Springer, Ronald
Zeitz, Heinz-Georg
Giese, Bernd
Chiral enolates 5 and 10, generated by radical addition and subsequent reduction, show diastereofacial selectivity during protonation.In the presence of substituted amines, diastereoselectivity is enhanced and becomes comparable to radical stereoselection
View MoreChangsha Kamer Essence and Flavor Co.,Ltd
Contact:86-731-89832270
Address:No.327 Kangnin Road Changsha Bio Information Industry Park, Changsha city, Hunan province
Hangzhou Neway Chemicals Co., Ltd.
Contact:+86-571-85095566
Address:Room 803, Qinglian Bldg, No 139 Qingchun Road, Hangzhou, Zhejiang China
Changsha Goomoo Chemical Technology Co.Ltd
Contact:+86-731-82197655
Address:No.649,Chezhan Rd.(N),Changsha,Hunan,China
Contact:+86-21-61318535
Address:Building 29,No.2139 Xizha Road, Fengxian District, Shanghai
Chengdu Green Young Biopharmaceutical INC
Contact:+86-28-85337952
Address:1-B-26,Tianhe Industry Park, No.1480 of Tianfu Road,Chengdu,P.R.China,610000
Doi:10.1016/j.tetasy.2012.01.006
(2012)Doi:10.1016/0008-6215(92)84178-U
(1991)Doi:10.1039/c2dt11752e
(2012)Doi:10.1016/j.bmc.2012.02.008
(2012)Doi:10.1134/S1070363211070310
(2011)Doi:10.1007/s13738-020-02041-7
(2021)