Issue 4, 2014

Nickel-mediated stereocontrolled synthesis of spiroketals via tandem cyclization–coupling of β-bromo ketals and aryl iodides

Abstract

A ketal-tether approach for the stereoselective synthesis of [5,5] and [5,6]-spiroketals based on reductive coupling catalyzed by the readily available Ni complex is demonstrated. Either an intermolecular or an intramolecular stereospecific cascade has been achieved as well.

Graphical abstract: Nickel-mediated stereocontrolled synthesis of spiroketals via tandem cyclization–coupling of β-bromo ketals and aryl iodides

Supplementary files

Article information

Article type
Communication
Submitted
10 Oct 2013
Accepted
01 Nov 2013
First published
04 Nov 2013

Chem. Commun., 2014,50, 472-474

Nickel-mediated stereocontrolled synthesis of spiroketals via tandem cyclization–coupling of β-bromo ketals and aryl iodides

Y. Peng, X. Xu, J. Xiao and Y. Wang, Chem. Commun., 2014, 50, 472 DOI: 10.1039/C3CC47780K

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