Unconventional Passerini Reaction toward α-Aminoxy-amides

  • Ajay L Chandgude
  • , Alexander Dömling*
  • *Corresponding author for this work

Research output: Contribution to journalLetter (Research letter)Academicpeer-review

30 Citations (Scopus)
125 Downloads (Pure)

Abstract

The Passerini multicomponent reaction (P-3CR) toward the one-step synthesis of α-aminoxy-amide, by employing for the first time a N-hydroxamic acid component, has been reported. The sonication-accelerated, catalyst-free, simple, fast, and highly efficient Passerini reaction is used for the synthesis of diverse α-aminoxy-amides. The reaction is compatible with a vast range of aldehydes, isocyanides, and N-hydroxamic acids such as N-hydroxysuccinimides and phthalimides. The generated Passerini products can be easily converted into several follow-up products.
Original languageEnglish
Pages (from-to)6396-6399
Number of pages4
JournalOrganic letters
Volume18
Issue number24
DOIs
Publication statusPublished - 16-Dec-2016

Keywords

  • MULTICOMPONENT REACTIONS
  • NORSTATINE ANALOGS
  • CYCLIC HEXAPEPTIDE
  • CHLORIDE-ION
  • ACIDS
  • PEPTIDES
  • PEPTIDOMIMETICS
  • FOLDAMERS
  • ISOCYANIDES
  • CHEMISTRY

Fingerprint

Dive into the research topics of 'Unconventional Passerini Reaction toward α-Aminoxy-amides'. Together they form a unique fingerprint.

Cite this