Arginine thioacid in synthesis of arginine conjugates and peptides

Siva S. Panda

doi:10.1039/c4ra04897k

Arginine thioacid in synthesis of arginine conjugates and peptides

Siva S. Panda

Chemistry and Physics

Research output: Contribution to journal › Article › peer-review

5 Scopus citations

Abstract

Protected arginine thioacid enables convenient N-acylation with no detectable racemization. We report efficient syntheses of potentially biologically active arginine conjugates and novel arginine-containing di-, tri- and tetrapeptides in good yields without loss of chiral integrity. This journal is

Original language	English (US)
Pages (from-to)	55210-55216
Number of pages	7
Journal	RSC Advances
Volume	4
Issue number	98
DOIs	https://doi.org/10.1039/c4ra04897k
State	Published - 2014

ASJC Scopus subject areas

Chemical Engineering(all)
Chemistry(all)

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10.1039/c4ra04897k

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abstract = "Protected arginine thioacid enables convenient N-acylation with no detectable racemization. We report efficient syntheses of potentially biologically active arginine conjugates and novel arginine-containing di-, tri- and tetrapeptides in good yields without loss of chiral integrity. This journal is",

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Arginine thioacid in synthesis of arginine conjugates and peptides

Abstract

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