Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 741 - 745 (1990)
Update date:2022-08-05
Topics: IR spectroscopy Regioselectivity Yield Catalyst Derivatives Steric hindrance Nucleophilic substitution TLC (thin-layer chromatography) NMR (nuclear magnetic resonance) Phenols Leaving group Workup Reaction Mechanism Solvent Effects Activation Energy Electrophilic Aromatic Substitution Byproduct Sulfenylation Trifluoromethyl group (–CF?)
Sizov, A. Yu
Kolomiets, A. F.
Fokin, A. V.
In the absence of a catalyst, α-trifluoromethyl-β-chloroethylsulfenyl chloride reacts electrophilically with ortho-para-substituted phenols bearing substituents of the first type.The reaction conditions are determined by the C-nucleophilic properties of t
View Moreshijiazhuang shuanglian chemical industry co.,ltd
Contact:0311-82190302
Address:Luquan Intersection , Shijiazhuang--Taiyuan Expressway，Shijiazhuang City
Hangzhou Showland Technology Co., Ltd.
Contact:86-571-88920516
Address:ROOM2118,NO.553,WENSAN ROAD,HANGZHOU,CHINA
Huaihua Baohua Biotechnology Co.,Ltd
website:http://www.baochengchem.com
Contact:86-519-82698291
Address:HouYang chemical development zone,Jintan,Jiangsu,China (213200)
SHANGHAI SYSTEAM BIOCHEM CO., LTD
website:http://www.systeambc.com
Contact:86-021-58380978
Address:Building 87，Lane 669， Dong Jing Road Shanghai,P.R.China
Wuhan Silworld Chemical Co.,Ltd
website:http://www.silworldchemical.com
Contact:+86-27-85613400
Address:No.198 jiangjun Road, Wuhan,China 430033
Doi:10.1248/cpb.38.839
(1990)Doi:10.1016/S0040-4020(99)00237-9
(1999)Doi:10.1007/s12640-019-00142-7
(2019)Doi:10.1002/anie.200907033
(2010)Doi:10.1134/S1070363215090042
(2015)Doi:10.1039/jr9510001851
(1951)
