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Royal Society of Chemistry, Chemical Science, 42(11), p. 11592-11600, 2020

DOI: 10.1039/d0sc04120c

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Forwards and backwards – synthesis of Laurencia natural products using a biomimetic and retrobiomimetic strategy incorporating structural reassignment of laurefurenynes C–F

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

The synthesis and structural reassignment of laurefurenynes C–F has been achieved, with the new structures fitting with a proposed biosynthesis. Also reported is the synthesis of ent-laurencin and ent-deacetyllaurencin via a retrobiomimetic approach.