Issue 45, 2020

Enantioselective total synthesis of (+)-ieodomycin A, (+)-ieodomycin B, and their three stereoisomers

Abstract

We describe a divergent and enantioselective total synthesis of (+)-ieodomycin A and (+)-ieodomycin B with three stereoisomers. The main advantage of the present synthesis is the late-stage elaboration of the side chain, which would afford a wide range of structurally diverse analogs with interesting bioactivities.

Graphical abstract: Enantioselective total synthesis of (+)-ieodomycin A, (+)-ieodomycin B, and their three stereoisomers

Supplementary files

Article information

Article type
Communication
Submitted
19 अक्तूबर 2020
Accepted
07 नवम्बर 2020
First published
09 नवम्बर 2020

Org. Biomol. Chem., 2020,18, 9227-9230

Enantioselective total synthesis of (+)-ieodomycin A, (+)-ieodomycin B, and their three stereoisomers

D. Choi, H. Choi, J. Lee, Y. Lee, H. Lee, J. M. Joo and J. S. Lee, Org. Biomol. Chem., 2020, 18, 9227 DOI: 10.1039/D0OB02107E

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