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

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