Arginine thioacid in synthesis of arginine conjugates and peptides

Research output: Contribution to journalArticle

3 Citations (Scopus)

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 languageEnglish (US)
Pages (from-to)55210-55216
Number of pages7
JournalRSC Advances
Volume4
Issue number98
DOIs
StatePublished - 2014

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Arginine
Peptides
Acylation

ASJC Scopus subject areas

  • Chemical Engineering(all)
  • Chemistry(all)

Cite this

Arginine thioacid in synthesis of arginine conjugates and peptides. / Panda, Siva S.

In: RSC Advances, Vol. 4, No. 98, 2014, p. 55210-55216.

Research output: Contribution to journalArticle

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