N-Iodosuccinimide as bifunctional reagent in (E)-selective C(sp2)−H sulfonylation of styrenes

Pramanik, Milan, Choudhuri, Khokan and Mal, Prasenjit 2018. N-Iodosuccinimide as bifunctional reagent in (E)-selective C(sp2)−H sulfonylation of styrenes. Asian Journal of Organic Chemistry 8 (1) , pp. 144-150. 10.1002/ajoc.201800644

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Abstract

Herein we report the use of N-iodosuccinimide (NIS) as a bifunctional reagent for a regio- and (E)-selective C(sp2)-H sulfonylation reaction of styrenes. Styrenes and sulfonyl hydrazides treated with NIS and potassium carbonate in ethanol at 70 °C resulted in (E)-vinyl sulfones exclusively with good to excellent yields. NIS, plays a dual role to generate sulfonyl radical from sulfonyl hydrazides at an initial stage and finally gives β-iodosulfone intermediate which was further converted to (E)-vinyl sulfones. Overall, a sustainable method for mild, metal free, convenient, one pot and direct synthesis of (E)-vinyl sulfones from styrenes are demonstrated via a C−S coupling reaction.

Item Type:	Article
Date Type:	Published Online
Status:	Published
Schools:	Chemistry
Publisher:	Wiley
ISSN:	2193-5807
Last Modified:	11 Jan 2023 12:42
URI:	https://orca.cardiff.ac.uk/id/eprint/155241

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