A mild and efficient CAN mediated oxidation of Morita–Baylis–Hillman adducts of 5-methyl-N-alkylisatin to 5-formyl-N-alkylisatin

Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/174

Full metadata record

DC Field	Value	Language
dc.contributor.author	Shanmugam, P	-
dc.contributor.author	Vaithiyanathan, V	-
dc.contributor.author	Selvakumar, K	-
dc.date.accessioned	2011-10-13T07:38:58Z	-
dc.date.available	2011-10-13T07:38:58Z	-
dc.date.issued	2008-03-24	-
dc.identifier.citation	Tetrahedron Letters 49(13):2119-2123;24 Mar 2008	en_US
dc.identifier.issn	0040-4039	-
dc.identifier.uri	http://hdl.handle.net/123456789/174	-
dc.description	Restricted Access	en_US
dc.description.abstract	A simple, mild and efficient CAN mediated oxidation of Morita–Baylis–Hillman adducts of 5-methyl-N-alkylisatins 1a–13a to 5-formyl-N-alkylisatins 1b–13b under ambient reaction conditions is reported. Simple and isomerized 5-methyl-N-alkylisatin derivatives 1–4 have also been tested and failed to provide the corresponding formylated products. A plausible reaction mechanism has been proposed.	en_US
dc.language.iso	en	en_US
dc.publisher	Elsevier	en_US
dc.subject	CAN	en_US
dc.subject	Morita–Baylis–Hillman adduct	en_US
dc.subject	Aryl methyl oxidation	en_US
dc.subject	Isatin	en_US
dc.subject	Aromatic aldehydes	en_US
dc.title	A mild and efficient CAN mediated oxidation of Morita–Baylis–Hillman adducts of 5-methyl-N-alkylisatin to 5-formyl-N-alkylisatin	en_US
dc.type	Article	en_US
Appears in Collections:	2008

Files in This Item:

File	Description	Size	Format
2008_0004.pdf Restricted Access		90.86 kB	Adobe PDF	View/Open Request a copy

DSpace JSPUI