Issue 17, 2021

Contemporary advancements in the semi-synthesis of bioactive terpenoids and steroids

Abstract

Many natural products have intriguing biological properties that arise from their fascinating chemical structures. However, the intrinsic complexity of the structural skeleton and the reactive functional groups on natural products pose tremendous challenges to chemical syntheses. Semi-synthesis uses chemical compounds isolated from natural sources as the starting materials to produce other novel compounds with distinct chemical and medicinal properties. In particular, advancements in various types of sp3 C–H bond functionalization reactions and skeletal rearrangement methods have contributed to the re-emergence of semi-synthesis as an efficient approach for the synthesis of structurally complex bioactive natural products. Here, we begin with a brief discussion of several bioactive natural products that were obtained via a semi-synthetic approach between 2008 and 2015 and we then discuss in-depth contemporary advancements in the semi-synthesis of bioactive terpenoids and steroids reported during 2016–2020.

Graphical abstract: Contemporary advancements in the semi-synthesis of bioactive terpenoids and steroids

Article information

Article type
Review Article
Submitted
08 mars 2021
Accepted
31 mars 2021
First published
31 mars 2021

Org. Biomol. Chem., 2021,19, 3791-3812

Contemporary advancements in the semi-synthesis of bioactive terpenoids and steroids

Z. Wang and C. Hui, Org. Biomol. Chem., 2021, 19, 3791 DOI: 10.1039/D1OB00448D

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