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 MoreContact:+86-633-8332928
Address:No.1,Huanghai Yilu.Rizhao,Shandong
Chongqing KonAo Health Co.,Ltd
Contact:13687578375
Address:wuhan hubei china
Shanghai Haoyuan Chemexpress Co., Ltd.
website:https://www.chemexpress.com/
Contact:86-21-58950125
Address:No.3 Building, No.1999, Zhangheng Road, ZhangjiangHighTech Park, Shanghai, P.R.China,201203
TIANJIN DONGRUXIANG MINERALS MARKETING CO.,LTD(expird)
Contact:22-58516360
Address:tianjin
Chengdu D-Innovation Pharmaceutical Co., Ltd
Contact:86-28-85105536
Address:1001, B6, No.88 Keyuan South Road, Chengdu Hi-Tech Zone
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)
