Russian Chemical Bulletin p. 492 - 499 (1995)
Update date:2022-09-26
Topics:
Grigorieva, N. Ya.
Pinsker, O. A.
Buevich, A. V.
Moiseenkov, A. M.
A highly-stereoselective method (90percent of the Z-isomer) was developed for the Peterson olefination of ketones with nerylacetone (1) as an example.The method is based on the introduction of a PhS group, which is removed after completion of the reaction, at the ketone C(3) atom. - Keywords: olefination of ketones, stereoselective synthesis, Peterson reaction, 2Z- and 2E-4-phenylthiofarnesoles and 2Z- and 2E-4-phenylthiofarnesoates
View MoreNanjing Vincero International Trading Co.,Ltd
Contact:8618936897229
Address:NO.68, ZhuShan Road, JiangNing WanDa Plaza, Building E Room 1703
Changsha Nutritopper Bio Technology Co.,Ltd.
Contact:+86-731-87803543
Address:East 1st Street, Baima Road, Ningxiang County
Anhui Biochem United Pharmaceutical Co., Ltd.
Contact:0086 551 5167062 / 5228268
Address:No. 30 Hongfeng Road, Hi-Tech Development Zone, Hefei (230088), China
Contact:0091-265-2313036
Address:311, ATLANTIS HEIGHTS SARABHAI MAIN ROAD,VADIWADI ,VADODARA
Taixing Shenfeng Chemical Co., Ltd.
Contact:+86-523-87117033, 87117666
Address:4# Yinsanlu, Huangqiao town, Taixing, Jiangsu, China.
Doi:10.1002/ps.2780420406
(1994)Doi:10.1016/j.ejmech.2014.03.019
(2014)Doi:10.1021/jo00095a040
(1994)Doi:10.1016/j.tet.2014.03.019
(2014)Doi:10.1039/c4cc01288g
(2014)Doi:10.1039/c4cc01254b
(2014)
