Issue 27, 2011

Stereospecificity in the Au-catalysed cyclisation of monoallylic diols. Synthesis of (+)-isoaltholactone

Abstract

We describe a concise synthesis of (+)-isoaltholactonevia a Au-catalysed cyclisation of a monoallylic diol to form the tetrahydrofuranyl ring. Analogous cyclisations show that the stereochemical outcome is dictated by the stereochemistry of the diol substrate.

Graphical abstract: Stereospecificity in the Au-catalysed cyclisation of monoallylic diols. Synthesis of (+)-isoaltholactone

Supplementary files

Article information

Article type
Communication
Submitted
30 Mar 2011
Accepted
25 May 2011
First published
10 Jun 2011

Chem. Commun., 2011,47, 7659-7661

Stereospecificity in the Au-catalysed cyclisation of monoallylic diols. Synthesis of (+)-isoaltholactone

W. P. Unsworth, K. Stevens, S. G. Lamont and J. Robertson, Chem. Commun., 2011, 47, 7659 DOI: 10.1039/C1CC11805F

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