Iron-catalyzed peroxidation-carbamoylation of alkenes with hydroperoxides and formamides: Via formyl C(sp2)-H functionalization

Jun Kee Cheng, Liang Shen, Liu Hai Wu, Xu Hong Hu*, Teck Peng Loh

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

33 Citations (Scopus)

Abstract

A reaction protocol in which FeCl3 and tert-butyl hydroperoxide facilitated a selective radical coupling reaction of aryl alkenes or 1,3-enynes with tert-butyl hydroperoxide and formamides to prepare an array of β-peroxy amides has been achieved. The β-peroxy amide could serve as a synthetic precursor which was facilely converted to β-hydroxy amide, β-keto amide and β-lactam following subsequent chemical transformation.

Original languageEnglish
Pages (from-to)12830-12833
Number of pages4
JournalChemical Communications
Volume53
Issue number95
DOIs
Publication statusPublished - 2017
Externally publishedYes

Bibliographical note

Publisher Copyright:
© The Royal Society of Chemistry 2017.

ASJC Scopus Subject Areas

  • Electronic, Optical and Magnetic Materials
  • Catalysis
  • Ceramics and Composites
  • General Chemistry
  • Surfaces, Coatings and Films
  • Metals and Alloys
  • Materials Chemistry

Fingerprint

Dive into the research topics of 'Iron-catalyzed peroxidation-carbamoylation of alkenes with hydroperoxides and formamides: Via formyl C(sp2)-H functionalization'. Together they form a unique fingerprint.

Cite this