Chemistry of Heterocyclic Compounds p. 56 - 59 (1994)
Update date:2022-08-04
Topics:
Sipyagin, A. M.
Pal'tsun, S. V.
Pomytkin, I. A.
Aleinikov, N. N.
The reaction on 2,3,5,6-tetrachloro-4-trifluoromethylthiopyridine with various nucleophilic reagents has been studied.It was shown that CF3S group is readily replaced under the action of O- and S-nucleophiles.Competition was detected between replacement of an α-chlorine atom on the pyridine ring and of the fluorine-containing group under the action of N-nucleophilic reagents.New derivatives of trichlorotrifluoromethylthiopyridine with nitrogen-containing substituents have been synthesized.
View Moreshijiazhuang baisheng chem co.; ltd
Contact:86-0311-80790826
Address:shijiazhuang hebei
WEIFANG DERUN CHEMICAL CO.,LTD
Contact:86-536-8956886
Address:weifang
Contact:86-10-62664360
Address:Building 10,No.18 AnNingZhuang East Road, GuangHua Pioneer Park,HaiDian District, BeiJing China
CHANGZHOU HANGYU PHARMACEUTICAL TECHNOLOGY CO., LTD
website:http://www.czyys.com
Contact:0086-519-88802789
Address:No.300,Yanling Middle Road, Changzhou, Jiangsu, China
LABTER PARMATECH(BEIJING)CO.,LTD
website:http://www.labter.com.cn/
Contact:+86-10-56330744
Address:NO.19,TIANRONG STREET,DAXING BIOMEDICIAL BASE ,ZHONGGUANCUN SCIENCE AND TECHNOLOGY PARK,BEIJING ,CHINA
Doi:10.1016/j.ejmech.2010.07.053
(2010)Doi:10.1016/j.ultsonch.2015.12.008
(2016)Doi:10.1021/acs.orglett.0c03507
(2020)Doi:10.1016/S0040-4039(99)01307-6
(1999)Doi:10.1021/ja00741a068
(1971)Doi:10.1016/S0022-328X(00)00622-7
(2001)
