Issue 46, 2013

Di- and triheteroarylalkanes via self-condensation and intramolecular Friedel–Crafts type reaction of heteroaryl alcohols

Abstract

An efficient synthetic approach to diheteroarylmethanes and 1,3-diheteroarylpropenes has been developed via Yb(III)-catalyzed sequential self-condensation of 2-furfuryl (or 2-thienyl or 3-indolyl) alcohols followed by intramolecular Friedel–Crafts type reaction and elimination of an aldehyde. This method offers a powerful entry and a potential alternative to the traditional synthesis of diheteroarylalkanes, which are precursors to the synthesis of several intriguing heteroaryls and more significantly, to the synthesis of biofuels.

Graphical abstract: Di- and triheteroarylalkanes via self-condensation and intramolecular Friedel–Crafts type reaction of heteroaryl alcohols

Supplementary files

Article information

Article type
Communication
Submitted
25 Sep 2013
Accepted
08 Oct 2013
First published
09 Oct 2013
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2013,11, 8030-8035

Di- and triheteroarylalkanes via self-condensation and intramolecular Friedel–Crafts type reaction of heteroaryl alcohols

S. Dhiman and S. S. V. Ramasastry, Org. Biomol. Chem., 2013, 11, 8030 DOI: 10.1039/C3OB41945B

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