Jump to main content
Jump to site search

Issue 17, 2013
Previous Article Next Article

Iodine-catalyzed tandem synthesis of terminal acetals and glycol mono esters from olefins

Author affiliations

Abstract

A new metal-free protocol is described for the synthesis of terminal acetals by tandem oxidative rearrangement of olefins using oxone as an oxidant in the presence of iodine. Moreover, a one-pot procedure for the preparation of glycol mono esters from olefins is also presented for the first time using the same reagent system.

Graphical abstract: Iodine-catalyzed tandem synthesis of terminal acetals and glycol mono esters from olefins

Back to tab navigation
Please wait while Download options loads

Supplementary files

Publication details

The article was received on 08 Nov 2012, accepted on 09 Jan 2013 and first published on 11 Jan 2013


Article type: Communication
DOI: 10.1039/C3CC38085H
Citation: Chem. Commun., 2013,49, 1711-1713
  •   Request permissions

    Iodine-catalyzed tandem synthesis of terminal acetals and glycol mono esters from olefins

    M. A. Kumar, P. Swamy, M. Naresh, M. M. Reddy, C. N. Rohitha, S. Prabhakar, A. V. S. Sarma, J. R. P. Kumar and N. Narender, Chem. Commun., 2013, 49, 1711
    DOI: 10.1039/C3CC38085H

Search articles by author