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Articles

Two ambuic acid dimers derived from homo-endo Diels-Alder reaction from Pestalotiopsis versicolor

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Pages 641-649 | Received 04 May 2022, Accepted 02 Oct 2022, Published online: 20 Oct 2022
 

Abstract

Two new dimers of ambuic acid, pestaloversicoloric acids A (1) and B (2), and a known derivative, 13(S)-hydroxyambuic acid (3), were isolated from the static fermentation product of Pestalotiopsis versicolor. The structural identification was accomplished via analyses on the data of HR-MS, 1 D and 2 D NMR, and ECD. Different from the well-known exo-type dimer, torreyanic acid, compounds 1 and 2 represent the first example of endo-type product derived from the intermolecular Diels-Alder reaction of two molecules of ambuic acid derivative with the identical absolute stereochemistry.

Disclosure statement

No potential conflict of interests was reported by the author(s).

Additional information

Funding

This work was sponsored by the Natural Science Foundation of Liaoning Province, China [Grant number 2019-ZD-0452].

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