Journal of the Chemical Society. Chemical communications p. 1753 - 1754 (1992)
Update date:2022-08-05
Topics: Optimization Retrosynthetic analysis Purification and characterization Functional group manipulation Scale-up Further Studies Ring Formation Radical Chemistry Safety and Ethical Considerations
Green, Stuart P.
Whiting, Donald A.
The keto-acid 5 undergoes stereospecific Peterson reaction to afford the (Z)-α-unsaturated ester-acid 6, and the derived phenyl selenoester cyclises also stereospecifically to the cis-hydrindanone 8 via a 5-exo acyl radical process; the ketone 8 is transformed through enone 11 into the diene-acids 2 and 3, models for study of C-18 radical reactions in steroid C/D systems.
View MoreGuangzhou Probig Fine Chemical Co., Ltd.
Contact:020-86297874
Address:No.2, 1/F, No.20, Hetai Road,Hebian Village, Baiyun District,Guangzhou,China
shanghai Tauto Biotech Co., Ltd
website:http://www.tautobiotech.com/en/index.htm
Contact:+86-21-51320588 ext. 8025
Address:No. 326, Aidisheng Rd , Zhangjiang Hi-tech Park, Shanghai , P.R.CHINA
Contact:86-571-87758773
Address:Room604 ,6F, Block A1-3 Xixi Plaza,No. 588 Wenyi West RD, Hangzhou,310012, China
Contact:21-7631221 15884421033
Address:326 Science and technology,Shanghai,China
Shenzhen JYMed Technology Co.,Ltd.
website:http://www.jymedtech.com
Contact:+86-755-26612112
Address:1#8,9/F, Biomedicine innovation Industrial Park, No.14, Jinhui Road, Pingshan Sistrict, Shenzhen, China
Doi:10.1021/jm00308a029
(1968)Doi:10.1016/j.bmcl.2005.03.052
(2005)Doi:10.1021/jo960568j
(1996)Doi:10.1016/S0022-328X(00)80082-0
(1969)Doi:10.1002/cphc.201100885
(2012)Doi:10.1016/S0040-4039(01)89937-8
(1967)
