Journal of Organic Chemistry p. 2212 - 2217 (1984)
Update date:2022-08-05
Topics: Synthesis Characterization NMR spectroscopy Chemical shift Synthetic route Hydroxy group Spectroscopic data Aryl group Purification Reaction yield 13C NMR
Rooney, C. S.
Cochran, D. W.
Ziegler, C.
Cragoe, E. J.
Williams, H. W. R.
5-Phenyl- and 5-thiazolyl-4-hydroxy-3(2H)-isothiazolone 1,1-dioxide derivatives have been prepared by base-catalyzed cyclocondensation of diethyl oxalate with an arylmethanesulfonamide, as well as by reaction of an arylmethanesulfonamide with methyl or et
View MoreSHANDONG CREDAGRI CHEMICAL CO., LTD.
Contact:+86-531-88872050
Address:ROOM 601A, BUILDING 2, SHUNTAI SQUARE, NO. 2000 SHUNHUA ROAD, HI-TECH DEVELOPMENT ZONE, JINAN, CHINA.
Shanghai Rainbow Chemistry Co., Ltd.
Contact:+86-21-64968086-5815/5812
Address:3rd floor, Building 7, 251 Faladi Road, Zhangjiang Hi-Tech Park, Pudong District, Shanghai, P.R. China
Shanghai Balmxy Pharmaceutical Co., Ltd
Contact:0086-21-24206007
Address:Room 402, 15#, No. 909 wangyue Road, shanghai, P. R. China
Anhui Dexinjia Biopharm Co., Ltd
Contact:+86-531-82375818
Address:9 Hexie Road, kaifaqu, Taihe
Changzhou Litong Chemical Co., Ltd.
website:http://www.litonchem.com/
Contact:+86-519-86301238
Address:Laoba Rd, Hutang town Changzhou Jiangsu
Doi:10.1021/ja00335a032
(1984)Doi:10.1021/jo00187a030
(1984)Doi:10.1002/anie.201903973
(2019)Doi:10.1021/ol0607847
(2006)Doi:10.1002/chem.202102347
(2021)Doi:10.1002/anie.200600458
(2006)
