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Synthesis 1995; 1995(5): 553-556
DOI: 10.1055/s-1995-3956
DOI: 10.1055/s-1995-3956
paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved.
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or duplication of any kind, translating, preparation of microfilms, and electronic
data processing and storage.A Simple and Efficient Preparation of 3-Aryl-3-Trifluoromethyl-3H-Diazirinyl Sulfoxides and Sulfones
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
31. Dezember 2000 (online)

All regioisomers of 3-aryl-3-trifluoromethyl-3H-diazirinyl sulfoxides and sulfones have been prepared in five steps from the corresponding bromothioanisoles in excellent overall yields. The key step involves a simultaneous oxidation of sulfide and diaziridine moieties respectively, to yield either the diazirine sulphoxide or sulphone, depending on reaction conditions.
diazirines - oxidation - sulfoxides - sulfones