Halocyclizations of Unsaturated Sulfoximines
Iodobenzene
DOI:
10.1021/acs.orglett.6b00958
Publication Date:
2016-05-11T11:57:44Z
AUTHORS (3)
ABSTRACT
A method for halocyclizations of S-alkenylsulfoximines is reported. When unsaturated NH-sulfoximines are treated with a combination iodobenzene diacetate and potassium iodide, transformation to the corresponding five- six-membered cyclic products occurs providing S-oxides dihydro isothiazoles tetrahydro-1,2-thiazines, respectively, in moderate high yields good diastereoselectivities excellent regioselectivities.
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