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FeBr3-catalyzed regioselective hydroxysulfenylation of N-allylsulfonamides with sulfonyl hydrazides

Abstract Regioselective hydroxysulfenylation of unactivated C C double bonds was reported. Using FeBr3-bpy as the catalyst, Na2S2O8 as the oxidant, and sulfonyl hydrazides as the sulfenyl sources, hydroxysulfenylation of unfunctionalized… Click to show full abstract

Abstract Regioselective hydroxysulfenylation of unactivated C C double bonds was reported. Using FeBr3-bpy as the catalyst, Na2S2O8 as the oxidant, and sulfonyl hydrazides as the sulfenyl sources, hydroxysulfenylation of unfunctionalized olefins proceeded readily, giving a variety of β-hydroxysulfides in moderate to good isolated yields.

Keywords: hydroxysulfenylation; regioselective hydroxysulfenylation; catalyzed regioselective; febr3 catalyzed; sulfonyl hydrazides; hydroxysulfenylation allylsulfonamides

Journal Title: Tetrahedron
Year Published: 2019

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