Morita–Baylis–Hillman reaction of indole-2-carboxaldehyde: new vistas for indole-annulated systems

Biswas, Subhasish; Singh, Virender; Batra, Sanjay

dc.contributor.author	Biswas, Subhasish
dc.contributor.author	Singh, Virender
dc.contributor.author	Batra, Sanjay
dc.date.accessioned	2011-06-07T05:39:24Z
dc.date.available	2011-06-07T05:39:24Z
dc.date.issued	2010
dc.identifier.citation	Tetrahedron,(2010),66(39),7781-7786	en
dc.identifier.uri	http://hdl.handle.net/123456789/684
dc.description.abstract	DABCO-mediated Morita-Baylis-Hillman reactions of several 1-substituted-indole-2-carboxaldehydes are disclosed. It was discovered that carboethoxy or tert-butoxycarbonyl groups installed at N-1 undergo cleavage under the reaction conditions to afford 2-substituted indoles. Utility of the N-substituted adducts for preparing a variety of annulated indoles has been exemplified.	en
dc.format.extent	380309 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	cdricommunicationno.7947	en
dc.subject	Morita-Baylis-Hillman	en
dc.subject	DABCO	en
dc.subject	indole-2-carboxaldehyde	en
dc.title	Morita–Baylis–Hillman reaction of indole-2-carboxaldehyde: new vistas for indole-annulated systems	en
dc.type	Article	en