Issue 42, 2015

The first total synthesis of (+)-goniothalesacetate and syntheses of (+)-altholactone, (+)-gonioheptolide A, and (−)-goniofupyrone by an asymmetric acetate aldol approach

Abstract

The first stereoselective total synthesis of (+)-goniothalesacetate and total synthesis of several bioactive styryl lactones, (+)-altholactone, (+)-gonioheptolide A, and (−)-goniofupyrone have been achieved from an advanced intermediate, which can be derived from L-(+)-DET.

Graphical abstract: The first total synthesis of (+)-goniothalesacetate and syntheses of (+)-altholactone, (+)-gonioheptolide A, and (−)-goniofupyrone by an asymmetric acetate aldol approach

Supplementary files

Article information

Article type
Paper
Submitted
31 Jul 2015
Accepted
21 Aug 2015
First published
24 Aug 2015

Org. Biomol. Chem., 2015,13, 10487-10495

Author version available

The first total synthesis of (+)-goniothalesacetate and syntheses of (+)-altholactone, (+)-gonioheptolide A, and (−)-goniofupyrone by an asymmetric acetate aldol approach

S. AnkiReddy, P. AnkiReddy and G. Sabitha, Org. Biomol. Chem., 2015, 13, 10487 DOI: 10.1039/C5OB01598G

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