Macrocyclic peptoids by selective s-acylation of cysteine esters

Mohamed A. Ibrahim, Siva S. Panda, Linda Nhon, Ahmed Hamed, Said A. El-Feky, Alan R. Katritzky

Research output: Contribution to journalArticle

3 Scopus citations

Abstract

Optimized selective S-acylations of cysteine esters gave intermediates for the synthesis of macrocyclic peptoids by a benzotriazole-based method.

Original languageEnglish (US)
Article numberSS-2012-M0856-OP
Pages (from-to)767-772
Number of pages6
JournalSynthesis (Germany)
Volume45
Issue number6
DOIs
StatePublished - 2013

Keywords

  • acylations
  • amino acids
  • heterocycles
  • macrocycles

ASJC Scopus subject areas

  • Organic Chemistry
  • Catalysis

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    Ibrahim, M. A., Panda, S. S., Nhon, L., Hamed, A., El-Feky, S. A., & Katritzky, A. R. (2013). Macrocyclic peptoids by selective s-acylation of cysteine esters. Synthesis (Germany), 45(6), 767-772. [SS-2012-M0856-OP]. https://doi.org/10.1055/s-0032-1318148