Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/xmlui/handle/10054/9333
Title: Application of the Suzuki-Miyaura cross-coupling reaction for the modification of phenylalanine peptides
Authors: KOTHA, S
LAHIN, K
Keywords: Amino-Acid Derivatives
Ring-Closing Metathesis
Diels-Alder Reaction
2+2+2 Cycloaddition Strategy
Enyne Metathesis
Tic Derivatives
Solid-Phase
Synthetic Approach
Chemical Synthesis
Drug Discovery
Issue Date: 2003
Publisher: JOHN WILEY & SONS INC
Citation: BIOPOLYMERS, 69(4), 517-528
Abstract: We have demonstrated an exceptionally simple and a useful methodology,for modification Of unusual phenylalanine peptides by adapting the building block approach using the Suzuki-Miyaura cross-coupling reaction as a key step. This strategy gave a good overall yield of various modified tri- and pentapeptides that may be useful to prepare various biologically active peptides in a short period of time. (C) 2003 .
URI: http://dx.doi.org/10.1002/bip.10420
http://dspace.library.iitb.ac.in/xmlui/handle/10054/9333
http://hdl.handle.net/10054/9333
ISSN: 0006-3525
Appears in Collections:Article

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