Issue 11, 2020

Total synthesis of isatindigotindoline C

Abstract

Total synthesis of isatindigotindoline C, a 3,3′-spiropyrrolidine oxindole alkaloid, is achieved in two steps using an exo-selective decarboxylative 1,3-dipolar cycloaddition as the key step. The synthesis verifies the originally assigned relative anti-stereochemistry for the bis-oxindole core of isatindigotindoline C.

Graphical abstract: Total synthesis of isatindigotindoline C

Supplementary files

Article information

Article type
Communication
Submitted
06 Ақп. 2020
Accepted
02 Нау. 2020
First published
02 Нау. 2020

Org. Biomol. Chem., 2020,18, 2051-2053

Author version available

Total synthesis of isatindigotindoline C

J. H. Siitonen, S. Lira, M. Yousufuddin and L. Kürti, Org. Biomol. Chem., 2020, 18, 2051 DOI: 10.1039/D0OB00270D

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