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

Department of Organic Chemistry, Indian Institute of Science, Bangalore, India 560012
Chemical Biology Units, JNCASR, Bangalore, India, 560012
Author to whom correspondence should be addressed.
Molecules 2007, 12(9), 2181-2189;
Received: 8 August 2007 / Accepted: 17 September 2007 / Published: 18 September 2007
(This article belongs to the Special Issue Bile Acids)
PDF [118 KB, uploaded 18 June 2014]


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. View Full-Text
Keywords: Hydrogel; Bile salt; Photodimerization; Acenaphthylene. Hydrogel; Bile salt; Photodimerization; Acenaphthylene.

Figure 1

This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

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Bhat, S.; Maitra, U. Hydrogels as Reaction Vessels: Acenaphthylene Dimerization in Hydrogels Derived from Bile Acid Analogues. Molecules 2007, 12, 2181-2189.

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