Please use this identifier to cite or link to this item: http://ir.niist.res.in:8080/jspui/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

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