Issue 12, 2014

Evidence that steric factors modulate reactivity of tautomeric iron–oxo species in stereospecific alkane C–H hydroxylation

Abstract

A new iron complex mediates stereospecific hydroxylation of alkyl C–H bonds with hydrogen peroxide, exhibiting excellent efficiency. Isotope labelling studies provide evidence that the relative reactivity of tautomerically related oxo–iron species responsible for the C–H hydroxylation reaction is dominated by steric factors.

Graphical abstract: Evidence that steric factors modulate reactivity of tautomeric iron–oxo species in stereospecific alkane C–H hydroxylation

Supplementary files

Article information

Article type
Communication
Submitted
11 Oct 2013
Accepted
01 Nov 2013
First published
04 Nov 2013
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2014,50, 1408-1410

Evidence that steric factors modulate reactivity of tautomeric iron–oxo species in stereospecific alkane C–H hydroxylation

M. Mitra, J. Lloret-Fillol, M. Haukka, M. Costas and E. Nordlander, Chem. Commun., 2014, 50, 1408 DOI: 10.1039/C3CC47830K

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