Issue 8, 2023

Synthesis of the ABC ring system of kadlongilactones

Abstract

A racemic approach towards the synthesis of the ABC (7/7/5) ring system of Schisandra triterpenoid kadlongilactones is described. The synthesis features two key transformations: (1) conjugate addition followed by iodolactonization to build the cis-fused 7/7 ring; and (2) conjugate addition–Rubottom oxidation cascade followed by ring-closing metathesis to construct the 7/7/5 tricyclic ring.

Graphical abstract: Synthesis of the ABC ring system of kadlongilactones

Supplementary files

Article information

Article type
Paper
Submitted
18 Sep 2022
Accepted
24 Jan 2023
First published
31 Jan 2023

Org. Biomol. Chem., 2023,21, 1704-1708

Synthesis of the ABC ring system of kadlongilactones

L. Li, P. Li, T. Li, M. Zhang, W. Liu, J. Li, L. Wang and Y. Chen, Org. Biomol. Chem., 2023, 21, 1704 DOI: 10.1039/D2OB01701F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements