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The Asymmetric Baylis-Hillman reaction: Use of chiral Michael acceptors, electrophiles, catalysts and the Lewis acid mediated isomerization of acetates of Baylis-Hillman adducts into trisubstituted alkenes

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Title The Asymmetric Baylis-Hillman reaction: Use of chiral Michael acceptors, electrophiles, catalysts and the Lewis acid mediated isomerization of acetates of Baylis-Hillman adducts into trisubstituted alkenes
 
Creator V., KANNAN
 
Subject Chemistry
 
Date 2004
 
Type Thesis
NonPeerReviewed
 
Format application/msword
 
Identifier http://eprints.csirexplorations.com/459/1/Abstract.doc
V., KANNAN (2004) The Asymmetric Baylis-Hillman reaction: Use of chiral Michael acceptors, electrophiles, catalysts and the Lewis acid mediated isomerization of acetates of Baylis-Hillman adducts into trisubstituted alkenes. PhD thesis, INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY HYDERABAD.
 
Relation http://eprints.csirexplorations.com/459/