Multicomponent reactions based on nucleophilic carbenes and their applications in organic synthesis

Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/3665

Full metadata record

DC Field	Value	Language
dc.contributor.author	Vijay Nair, G	-
dc.contributor.author	Rajeev S Menon	-
dc.contributor.author	Sreekumar, V	-
dc.date.accessioned	2021-02-08T13:32:23Z	-
dc.date.available	2021-02-08T13:32:23Z	-
dc.date.issued	2005	-
dc.identifier.citation	Pure and Applied Chemistry 77(7):1191-1198; Jul 2005	en_US
dc.identifier.issn	0033-4545	-
dc.identifier.uri	http://hdl.handle.net/123456789/3665	-
dc.description.abstract	Zwitterionic intermediates generated from the addition of nonprotic nucleophiles to activated acetylenes are intercepted with various third components constituting novel multicomponent organic transformations. Catalytic amounts of an organic base like pyridine were found to trigger reactions between an electrophilic acetylene and a variety of electrophiles. The reactions proceed through dipolar intermediates and show high stereoselectivity.	en_US
dc.language.iso	en	en_US
dc.publisher	Walter de Gruyter	en_US
dc.subject	Carbenes	en_US
dc.subject	Multicomponent reactions	en_US
dc.subject	Isocyanides	en_US
dc.subject	Dipoles	en_US
dc.subject	Zwitterions	en_US
dc.title	Multicomponent reactions based on nucleophilic carbenes and their applications in organic synthesis	en_US
dc.type	Article	en_US
Appears in Collections:	2005

Files in This Item:

File	Description	Size	Format
2005_0104.pdf Restricted Access		256.12 kB	Adobe PDF	View/Open Request a copy

DSpace JSPUI