
Journal of the American Chemical Society p. 134 - 144 (1989)
Update date:2022-08-05
Topics:
Pearson, Anthony J.
Blystone, Sheri L.
Nar, Herbert
Pinkerton, A. Alan
Roden, Brian A.
Yoon, Jaeyon
Asymmetric induction as high as 90percent ee was obtained during the reaction of enolates, derived from optically pure sulfoximinyl esters of type 16, with the cycloheptadiene-Mo(CO)2Cp cation.Lower, but still significant asymmetric induction was observed
View Morewebsite:http://www.tbbmed.com
Contact:86--21-50498136
Address:Room 6002, Building 7-1, No.160 Basheng Road,Pudong Area,Shanghai China
Zhengzhou Yuanli Biological Technology Co., Ltd.
Contact:+86-371-67897870/67897895
Address:No. 38, Qingyang Street, Zhengzhou, Henan, China
Hangzhou Eastbiopharm Co.,Ltd.
Contact:+86-571-88931780
Address:Hangzhou,China
Qingdao Kylin Trading Co., Ltd.
Contact:0086-532-68979884/58972912/68972263/65/88171519
Address:Room 2308,A building International Trade Center No.230 Changjiang Middle Road of Qingdao Economic Development Zone,Shandong,China.
Kaymossy BioChem Tech Co., Ltd
website:http://www.kaimosi.com
Contact:0571-87191913/0571-87199097
Address:Room 215, Building 3rd, No.288 Ningxia Road, Qingdao city, China
Doi:10.1021/ja00163a044
(1990)Doi:10.1021/ja00906a017
(1963)Doi:10.1002/ejoc.200800714
(2008)Doi:10.1039/c9ob01530b
(2019)Doi:10.1139/v81-383
(1981)Doi:10.1021/acs.joc.8b02676
(2018)