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
AUTHORS (5)
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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