Bulletin of the Chemical Society of Japan p. 1795 - 1798 (1983)
Update date:2022-09-26
Topics:
Akiyama, Takeo
Yoshida, Yasuki
Hanawa, Tokiko
Sugimori, Akira
The treatment of 1,1,1,3-tetrachloro-3-phenylpropane with alkali in ethanol affords ethynyl phenyl ketone and its acetal in good yields.This reaction proceeds through the elimination of hydrogen chloride and an efficient 1,3-proton transfer catalyzed by base.Ethyl cinnamate is obtained in only 2percent yield.
View MoreNanjing Spring & Autumn Biological Engineering Co., Ltd.
Contact:86-180510-83338
Address:Suite# 210, No. 1 BuildingNanjing Agricultural Biotechnology High-tech Entrepreneurship Center, No. 4 Tongwei Road, Xuanwu District, Nanjing,China
Contact:+86-535-8888888
Address:No.161 Haishi Rd.
website:https://www.bocsci.com/
Contact:1-631-485-4226
Address:Ramsey Road
Contact:86-574-26865651
Address:529 YuanBaoShan Road, Beilun District
Hangzhou Bayee Chemical Co.,Ltd.
Contact:+86-571-86990109
Address:No.380, Jiangnan Auenue, Binjiang District, Hangzhou, China
Doi:10.1021/ja00361a047
(1983)Doi:10.1021/ja00364a045
(1983)Doi:10.1021/ja056458o
(2006)Doi:10.1021/jo052077h
(2006)Doi:10.1021/ja00314a026
(1984)Doi:10.1039/c4cc00024b
(2014)
