Iodine-catalyzed three-component oxysulfenylation of alkenes with sulfonyl hydrazides and alcohols.
نویسندگان
چکیده
An unprecedented three-component oxysulfenylation reaction of alkenes with sulfonyl hydrazides and alcohols has been developed in the presence of 20 mol% iodine to give a range of structurally diverse β-alkoxy sulfides in good to excellent yields.
منابع مشابه
Iodine-catalyzed thiolation of electron-rich aromatics using sulfonyl hydrazides as sulfenylation reagents.
Iodine-catalyzed thiolation of electron-rich aromatics, including substituted anisole, thioanisole, phenol, toluene, and naphthalene, using sulfonyl hydrazides as sulfenylation reagents was carried out. Sulfonothioates, the products of decomposition of sulfonyl hydrazides in the presence of iodine, are proposed as the major sulfenylation species in this transformation.
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ورودعنوان ژورنال:
- Chemical communications
دوره 50 17 شماره
صفحات -
تاریخ انتشار 2014