Issue 33, 2022

First synthesis of an ABCE ring substructure of daphnicyclidin A

Abstract

The ABCE tetracyclic ring system of daphnicyclidin A was prepared using an intramolecular (4 + 3) cycloaddition of an oxidopyridinium ion as the key step. This route consists of a 10-step synthesis with an overall yield of 20.2%. This result offers support for the use of this strategy for total synthesis of daphnicyclidin A.

Graphical abstract: First synthesis of an ABCE ring substructure of daphnicyclidin A

Supplementary files

Article information

Article type
Communication
Submitted
11 Jul 2022
Accepted
28 Jul 2022
First published
29 Jul 2022

Org. Biomol. Chem., 2022,20, 6547-6549

Author version available

First synthesis of an ABCE ring substructure of daphnicyclidin A

J. Tu, M. M. Clark and M. Harmata, Org. Biomol. Chem., 2022, 20, 6547 DOI: 10.1039/D2OB01246D

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