An Iodine‐Mediated Hofmann‐Löffler‐Freytag Reaction of Sulfoximines Leading to Dihydroisothiazole Oxides

01 natural sciences 0104 chemical sciences
DOI: 10.1002/adsc.201701178 Publication Date: 2017-10-02T02:28:43Z
ABSTRACT
AbstractA Hofmann‐Löffler‐Freytag type cyclization reaction of S‐aryl‐S‐phenylpropyl sulfoximines (and related derivatives) was developed. Using molecular iodine as the initiator under visible light a series of five‐membered cyclic products was obtained in moderate to high yields. The approach represents a new strategy for the synthesis of dihydroisothiazole oxides and benzo[d]isothiazoles‐1‐oxides.magnified image
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