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DESIGN AND SYNTHESIS OF CONFORMATIONALLY CONSTRAINED BICYCLO[2.2.2]OCTANE-BASED UNUSUAL alpha-AMINO ACID DERIVATIVES VIA THE DIELS-ALDER REACTION

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Title DESIGN AND SYNTHESIS OF CONFORMATIONALLY CONSTRAINED BICYCLO[2.2.2]OCTANE-BASED UNUSUAL alpha-AMINO ACID DERIVATIVES VIA THE DIELS-ALDER REACTION
 
Creator KOTHA, S
MESHRAM, M
 
Subject CARBOXYLIC-ACIDS
9-SUBSTITUTED ANTHRACENES
FUNCTIONAL-GROUPS
REDUCTION
ALCOHOLS
METATHESIS
PEPTIDES
Bicyclic alpha-Amino Acid Derivative
Anthracene Derivative
o-Quinodimethane
Diels-Alder Reaction
Glycine Equivalent
 
Description We report a simple synthetic approach to various conformationally constrained bicyclic alpha-amino acid derivatives using the Diels-Alder reaction as a key step. Moreover, we have investigated the reactivity pattern of various anthracene derivatives in relation to the Diels-Alder chemistry.
 
Publisher PERGAMON-ELSEVIER SCIENCE LTD
 
Date 2016-01-15T10:41:18Z
2016-01-15T10:41:18Z
2015
 
Type Article
 
Identifier HETEROCYCLES, 90(1)357-371
0385-5414
1881-0942
http://dx.doi.org/10.3987/COM-14-5(K)26
http://dspace.library.iitb.ac.in/jspui/handle/100/18372
 
Language en