CuBr/TBHP-Mediated Synthesis of N-Acyl Sulfonimidamides Via the Oxidative Cross-coupling of Sulfonimidamides and Aldehydes

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DC Field	Value	Language
dc.contributor.author	Nandi, G C	-
dc.contributor.author	Raju, C	-
dc.date.accessioned	2018-07-31T09:16:07Z	-
dc.date.available	2018-07-31T09:16:07Z	-
dc.date.issued	2017-02-03	-
dc.identifier.citation	Organic and Biomolecular Chemistry, 15(10):2234-2239	en_US
dc.identifier.uri	http://10.10.100.66:8080/xmlui/handle/123456789/3234	-
dc.description.abstract	N-Acyl sulfonimidamides were synthesized via a Cu-catalyzed double C–H/N–H activation protocol. The imino end of sulfonimidamides was acylated using aldehyde as the acylating agent and t-butyl hydrogen peroxide (TBHP) as the oxidant in acetonitrile (MeCN) at 82 °C. The mild reaction conditions afforded low-to-moderate yields of N-acyl sulfonimidamides with high structural diversity.	en_US
dc.language.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.title	CuBr/TBHP-Mediated Synthesis of N-Acyl Sulfonimidamides Via the Oxidative Cross-coupling of Sulfonimidamides and Aldehydes	en_US
dc.type	Article	en_US
Appears in Collections:	2017

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