
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 MoreChengda Pharmaceuticals Co., Ltd.
Contact:+86-573-84601188
Address:hengshan Road 5# in Jiashan, zhejiang
FUJIAN SHANSHUI CHEMICAL CORP.LTD.
Contact:+86-151-59920036
Address:Jinqiao Gareden, jo@fj-xinyi.com
LianYunGang Chiral Chemical(CHINA) CO.,LTD
Contact:+86-518-83616958 +86-519-82884848
Address:LianYunGang Chemical Industry Park (JiangSu)
Dezhou Longteng Chemical Co., Ltd.
website:http://www.sodium-methoxide.cn/
Contact:0086-18866052283
Address:Xinhua Industrial Zone, Dezhou City, Shandong Province, China
AUSHUN PHARMACEUTICAL TECHNOLOGY CO,.LTD
Contact:+86-25-86883560 15951806178
Address:14 Dayingbi, Zhujiang Rd. East, Nanjing, Jiangsu, China.
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)