1,3-Dipolar cycloadditions of nonstabilised azomethine ylides at 3-substituted coumarins: Synthesis of 1-benzopyrano[3,4-c]pyrrolidines

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Title:	1,3-Dipolar cycloadditions of nonstabilised azomethine ylides at 3-substituted coumarins: Synthesis of 1-benzopyrano[3,4-c]pyrrolidines
Authors:	Moshkin, Vladimir S. Sosnovskikh, Vyacheslav Ya. Slepukhin, Pavel A. Röschenthaler, Gerd Volker
Issue Date:	2012
Citation:	1,3-Dipolar cycloadditions of nonstabilised azomethine ylides at 3-substituted coumarins: Synthesis of 1-benzopyrano[3,4-c]pyrrolidines / Vladimir S. Moshkin, Vyacheslav Ya. Sosnovskikh, Pavel A. Slepukhin, Gerd Volker Röschenthaler // Mendeleev Communications. — 2012. — Vol. 22. — № 1. — P. 29-31.
Abstract:	Reaction of 3-substituted coumarins with N-alkyl-α-amino acids and aldehydes proceeds regio- and stereoselectively to give 1-benzopyrano[3,4-c] pyrrolidines as a result of 1,3-dipolar cycloaddition of the intermediate azomethine ylides at the Δ 3-bond of the coumarins. © 2012 Mendeleev Communications. All rights reserved.
URI:	http://elar.urfu.ru/handle/10995/50920
Access:	info:eu-repo/semantics/restrictedAccess
RSCI ID:	17975292
SCOPUS ID:	84856557887
WOS ID:	000301020400011
PURE ID:	1128462
ISSN:	0959-9436
DOI:	10.1016/j.mencom.2012.01.011
Appears in Collections:	Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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