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Synthesis of a conformationally constrained phenylalanine derivative by a strategic combination of ring-closing enyne metathesis and Diels-Alder reaction

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Title Synthesis of a conformationally constrained phenylalanine derivative by a strategic combination of ring-closing enyne metathesis and Diels-Alder reaction
 
Creator KOTHA, S
KHEDKAR, P
 
Subject acid tic derivatives
pictet-spengler reaction
1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
amino-acids
asymmetric-synthesis
napieralski reaction
peptide antagonists
heck cyclizations
receptor
design
constrained amino acid
phenylalanine
ring closure
metathesis
diets-alder
 
Description An efficient route towards the synthesis of a conformationally constrained phenylalanine derivative is demonstrated using the strategic combination of ring-closing enyne metathesis and Diels-Alder reaction as key steps.
 
Publisher GEORG THIEME VERLAG KG
 
Date 2011-07-30T08:50:10Z
2011-12-26T12:52:45Z
2011-12-27T05:39:37Z
2011-07-30T08:50:10Z
2011-12-26T12:52:45Z
2011-12-27T05:39:37Z
2008
 
Type Article
 
Identifier SYNTHESIS-STUTTGART, (18), 2925-2928
0039-7881
http://dx.doi.org/10.1055/s-2008-1067237
http://dspace.library.iitb.ac.in/xmlui/handle/10054/7908
http://hdl.handle.net/10054/7908
 
Language en