Studies on the reactivity of calix[4]arene derived bis(spirodienone) with carbo- and hetero-dienophiles and dichlorocarbene: synthesis of highly functionalized macrocycles

Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1689

Title:	Studies on the reactivity of calix[4]arene derived bis(spirodienone) with carbo- and hetero-dienophiles and dichlorocarbene: synthesis of highly functionalized macrocycles
Authors:	Ganga, V B Sreeja, T Suresh, E Luxmi Varma, R
Keywords:	Diels-alder reaction C-nitrosocarbonyl compounds Acylnitroso dienophiles Spirodienone route Calixarenes
Issue Date:	2007
Publisher:	Elsevier
Citation:	Tetrahedron 63(19):4134-4143;7 May 2007
Abstract:	Calix[4]arene derived bis(spirodienone) can act as a 4 pi component in cycloaddition reaction with a variety of carbo- and heterodienophiles yielding the bisadducts in excellent to quantitative yields. Bis(spirodienone) also undergoes addition reactions with dichlorocarbene resulting in mono- and bis-dichlorocyclopropyl derived bis(spiroenones) in excellent yields.
URI:	http://ir.niist.res.in:8080/jspui/handle/123456789/1689
ISSN:	0040-4020
Appears in Collections:	2007

Files in This Item:

File	Description	Size	Format
2007_00171.pdf Restricted Access		1.39 MB	Adobe PDF	View/Open Request a copy

DSpace JSPUI