An Efficient Route to N-Monosubstituted Guanidino-Lactams

Sara Tommasi*, Chiara Zanato, Rey Carabeo, Arduino Mangoni, Sergio Dall'Angelo, Matteo Zanda

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)
8 Downloads (Pure)

Abstract

A small library of guanidino-lactams were synthesized in four steps and good overall yields by following the routes: preparation of guanylating agents, synthesis of protected guanidino-acids, cyclization to fully protected guanidino-lactams, and deprotection to the target compounds. The guanidino-lactams were assayed as antimicrobials on E. coli showing no significant antibiotic activity.
Original languageEnglish
Article numberss-2015-n0113-op
Pages (from-to)3067-3078
Number of pages12
JournalSynthesis
Volume47
Issue number19
Early online date25 Jun 2015
DOIs
Publication statusPublished - Oct 2015

Keywords

  • guanidines
  • guanylation
  • lactams
  • cyclization
  • antimicrobials

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