Issue 39, 2014

Iron-catalysed asymmetric tandem spiro-cyclization using dioxygen in air as the hydrogen acceptor

Abstract

A tandem combination of ortho-quinone methide (o-QM) formation/Michael addition/asymmetric dearomatization, which is catalysed by an iron–salan complex in air with high enantioselectivity, provides an efficient method for spirocyclic (2H)-dihydrobenzofuran synthesis from 2-naphthols and phenols. The key to the success of the tandem synthesis is the development of aerobic oxidative o-QM formation.

Graphical abstract: Iron-catalysed asymmetric tandem spiro-cyclization using dioxygen in air as the hydrogen acceptor

Supplementary files

Article information

Article type
Communication
Submitted
01 Mar 2014
Accepted
26 Mar 2014
First published
26 Mar 2014

Chem. Commun., 2014,50, 5053-5056

Author version available

Iron-catalysed asymmetric tandem spiro-cyclization using dioxygen in air as the hydrogen acceptor

T. Oguma and T. Katsuki, Chem. Commun., 2014, 50, 5053 DOI: 10.1039/C4CC01555J

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