Synthesis of bisindoles scaffolds by palladium-catalyzed allylic alkylation of N-aminoindole with ortho-iodoaryl allenes

Abstract

A highly efficient Pd-catalyzed domino allylic alkylation of ortho-iodoaryl allenes with N-aminoindoles has been developed. This protocol enables the synthesis of a variety of diversely substituted N−N scaffold-containing bisindoles under mild reaction conditions. The method features broad substrate scope, good functional group tolerance, and high chemoselectivity, allowing the simultaneous formation of C−C and C−N bonds in a single step

Supplementary files

Article information

Article type
Communication
Submitted
18 Mar 2026
Accepted
29 Apr 2026
First published
29 Apr 2026

Org. Biomol. Chem., 2025, Accepted Manuscript

Synthesis of bisindoles scaffolds by palladium-catalyzed allylic alkylation of N-aminoindole with ortho-iodoaryl allenes

C. Ding, Y. Yin, E. Hu, H. Dong, Y. He, S. Wu, Y. Han and L. Wang, Org. Biomol. Chem., 2025, Accepted Manuscript , DOI: 10.1039/D6OB00447D

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