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Hydrogels as Reaction Vessels: Acenaphthylene Dimerization in Hydrogels Derived from Bile Acid Analogues

Bhat, Shreedhar and Maitra, Uday (2007) Hydrogels as Reaction Vessels: Acenaphthylene Dimerization in Hydrogels Derived from Bile Acid Analogues. In: Molecules, 12 (9). pp. 2181-2189.

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Official URL: http://www.mdpi.com/1420-3049/12/9/2181

Abstract

Many chemical reactions which are otherwise clean often lead to the formation of multiple products. Such products may be formed due to a lack of chemo-, regio- and/or stereoselectivity. For such reactions to be useful, one should be able to control them to yield a single desired product. Of the many approaches used in this context, the use of reaction media with features different from those of isotropic solutions has been very effective. Surfactant micelles have been shown to control the product selectivity in photochemical reactions, but the dynamic nature of the micelles probably results in differential effects on reaction selectivity. In this article we provide the results on photodimerization reactions performed in bile salt gels.

Item Type: Journal Article
Additional Information: Copyright of this article belongs to Molecular Diversity Preservation International.
Keywords: Hydrogel;Bile salt;Photodimerization;Acenaphthylene.
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Date Deposited: 18 Dec 2008 03:49
Last Modified: 19 Sep 2010 04:52
URI: http://eprints.iisc.ernet.in/id/eprint/16539

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