Synthesis of functionalized 3-spirocyclopropane-2-indolones from isomerised Baylis-Hillman adducts of isatin

dc.contributor.author	Shanmugam, P
dc.contributor.author	Vaithyanathan, V
dc.contributor.author	Viswambharan, B
dc.date.accessioned	2016-01-18T07:58:49Z
dc.date.available	2016-01-18T07:58:49Z
dc.date.issued	2006
dc.identifier.citation	Tetrahedron 62(18):4342-4348; May 2006	en_US
dc.identifier.issn	0040-4020
dc.identifier.uri	http://ir.niist.res.in:8080/jspui/handle/123456789/2170
dc.description.abstract	A facile, high yield stereoselective synthesis of functionalized diastereomeric 3 -spirocyclopropane-2-indolones (10-17a,b) from the isomerised bromo derivatives of Baylis-Hillman adducts of isatin(2-9a,b) by reductive cyclization with sodium borohydride is reported	en_US
dc.language.iso	en	en_US
dc.publisher	Elsevier	en_US
dc.subject	Isatin	en_US
dc.subject	Spirocyclopropane	en_US
dc.subject	Sodium borohydride	en_US
dc.subject	2-indalones	en_US
dc.subject	Baylis Hillman adduct	en_US
dc.subject	Vinyl radical cyclization	en_US
dc.subject	Diels alder reaction	en_US
dc.subject	Stereoselective synthesis	en_US
dc.subject	Assisted isomerization	en_US
dc.subject	Alkenes	en_US
dc.title	Synthesis of functionalized 3-spirocyclopropane-2-indolones from isomerised Baylis-Hillman adducts of isatin	en_US
dc.type	Article	en_US