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Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/2170
Title: Synthesis of functionalized 3-spirocyclopropane-2-indolones from isomerised Baylis-Hillman adducts of isatin
Authors: Shanmugam, P
Vaithyanathan, V
Viswambharan, B
Keywords: Isatin
Spirocyclopropane
Sodium borohydride
2-indalones
Baylis Hillman adduct
Vinyl radical cyclization
Diels alder reaction
Stereoselective synthesis
Assisted isomerization
Alkenes
Issue Date: 2006
Publisher: Elsevier
Citation: Tetrahedron 62(18):4342-4348; May 2006
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
URI: http://ir.niist.res.in:8080/jspui/handle/123456789/2170
ISSN: 0040-4020
Appears in Collections:2006

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