Oxidant controlled regioselective mono- and di-functionalization reactions of coumarins

Chem Commun (Camb). 2015 Oct 28;51(84):15422-5. doi: 10.1039/c5cc06200d.

Abstract

C-3 alkylation of coumarins has been accomplished using cycloalkanes or alkylbenzenes in the presence of di-tert-butylperoxide (DTBP) and Fe(III) catalyst. Under metal free conditions and just by switching the oxidant from DTBP to TBHP, an exclusive C-4 cycloalkylation-C-3 peroxidation reaction takes place. During C-3 alkylation, the C-C bond formation occurs at the expense of an existing C-C bond, while the C-4 alkylation is associated with the formation of new C-C and C-O bonds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylation
  • Coumarins / chemistry*
  • Molecular Structure
  • Oxidants / chemistry*
  • Peroxides / chemistry*
  • Stereoisomerism
  • tert-Butylhydroperoxide / chemistry*

Substances

  • Coumarins
  • Oxidants
  • Peroxides
  • di-tert-butyl peroxide
  • tert-Butylhydroperoxide