Issue 41, 2018

First enantioselective total synthesis of altersolanol A

Abstract

The first enantioselective total synthesis of altersolanol A, a secondary metabolite from the endophytic fungi Stemphylium globuliferum and Alternaria solani, is described. The key step towards the tetrahydroanthraquinone core was an asymmetric DielsAlder (D–A) cycloaddition promoted by (R)-3,3′-diphenyl-BINOL/boron Lewis acid with good to excellent yields and excellent diastereo- and enantioselectivity (>95 : 5 dr and 98 : 2 er).

Graphical abstract: First enantioselective total synthesis of altersolanol A

Supplementary files

Article information

Article type
Paper
Submitted
28 Aug 2018
Accepted
28 Sep 2018
First published
01 Oct 2018

Org. Biomol. Chem., 2018,16, 7674-7681

First enantioselective total synthesis of altersolanol A

B. Mechsner, B. Henßen and J. Pietruszka, Org. Biomol. Chem., 2018, 16, 7674 DOI: 10.1039/C8OB02113A

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