Synthesis

Convenient one-pot procedure for converting aryl sulfides to nitroaryl sulfones

M Nose, H Suzuki

Index: Nose, Masatoshi; Suzuki, Hitomi Synthesis, 2002 , # 8 p. 1065 - 1071

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Citation Number: 12

Abstract

Abstract When treated with nitrogen dioxide and ozone in inert solvent at 0 C or below, aryl sulfides underwent smooth oxidative nitration to give nitroaryl sulfones in good yield. Using this methodology, a series of mono-and di-nitrated aryl sulfones were prepared from methyl phenyl sulfide and diphenyl sulfide and their physical data are presented.

Synthese von 2??substituiertem 2, 3??Dihydro??1H??dibenzo [b, f] pyrazolo [1, 2??d][1, 4, 5] thiadiazepin??9??dioxid??1, 3??dion. Über Pyrazole, 2. Mitteilung

[Michel,K.; Matter,M. Helvetica Chimica Acta, 1961 , vol. 44, p. 2204 - 2208]

2-Amino-6-arylsulfonylbenzonitriles as non-nucleoside reverse transcriptase inhibitors of HIV-1

[Chan; Hong; Hunter III; Orr; Cowan; Sherman; Sparks; Reitter; Andrews III; Hazen; St. Clair; Boone; Ferris; Creech; Roberts; Short; Weaver; Ott; Ren; Hopkins; Stuart; Stammers Journal of Medicinal Chemistry, 2001 , vol. 44, # 12 p. 1866 - 1882]

2-Amino-6-arylsulfonylbenzonitriles as non-nucleoside reverse transcriptase inhibitors of HIV-1

Convenient one-pot procedure for converting aryl sulfides to nitroaryl sulfones

Abstract

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