Facile assembly of 1,5-diazocan-2-ones: via cyclization of tethered sulfonamides to cyclopropenes

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DC Field	Value	Language
dc.contributor.author	Rubin, M. A.	-
dc.contributor.author	Рубин, М. А.	-
dc.date.accessioned	2021-01-20T12:43:43Z	-
dc.date.available	2021-01-20T12:43:43Z	-
dc.date.issued	2020	-
dc.identifier.citation	Matheny, J.P., Yamanushkin, P.M., Petillo, P.A., Rubin, M. Facile assembly of 1,5-diazocan-2-ones: via cyclization of tethered sulfonamides to cyclopropenes // RSC Advances. - 2020. - Volume 10. - Issue 72. - Pages 44183-44190	ru
dc.identifier.uri	http://hdl.handle.net/20.500.12258/14756	-
dc.description.abstract	The sulfonamide moiety was evaluated as an activating and stabilizing functional group in the metal-templated strain release-driven intramolecular nucleophilic addition of amines to cyclopropenes to generate 1,5-diazocan-2-ones	ru
dc.language.iso	en	ru
dc.publisher	Royal Society of Chemistry	ru
dc.relation.ispartofseries	RSC Advances	-
dc.subject	Addition reactions	ru
dc.subject	Amides	ru
dc.subject	Amines	ru
dc.subject	Sulfur compounds	ru
dc.title	Facile assembly of 1,5-diazocan-2-ones: via cyclization of tethered sulfonamides to cyclopropenes	ru
dc.type	Статья	ru
vkr.inst	Химико-фармацевтический факультет	ru
Appears in Collections:	Статьи, проиндексированные в SCOPUS, WOS

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