http://dx.doi.org/10.1016/j.tetlet.2010.06.097">
 

Document Type

Journal Article

Department/Unit

Department of Chemistry

Title

Highly efficient synthesis of extended triptycenes via Diels–Alder cycloaddition in water under microwave radiation

Language

English

Abstract

Microwave-irradiated Diels-Alder reactions of anthracene and endoxides (6a-g) in water afforded the cycloadducts (8a-g) with high efficiencies. The extended triptycenes (2a-g) were readily obtained by dehydration of 8a-g in a mixture of AcOH and Ac2O with good overall yields. © 2010 Elsevier Ltd. All rights reserved.

Keywords

Dehydration, Diels-Alder cycloaddition, Endoxides, Extended triptycene, Microwave

Publication Date

2010

Source Publication Title

Tetrahedron Letters

Volume

51

Issue

34

Start Page

4519

End Page

4522

Publisher

Elsevier

ISSN (print)

00404039

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