Issue 10, 2019

Palladium-catalyzed dearomative arylphosphorylation of indoles

Abstract

A palladium-catalyzed dearomative arylphosphorylation reaction of indoles involving C–C/C–P bond formation is developed. Through the intramolecular dearomative carbopalladation of indoles followed by an intermolecular benzyl–Pd termination with dialkylphosphite, a range of unique indolines bearing vicinal tetrasubstituted and phosphate-containing trisubstituted stereocenters are obtained in good yields. Synthetic transformations of the product show practical utilities of the reaction.

Graphical abstract: Palladium-catalyzed dearomative arylphosphorylation of indoles

Supplementary files

Article information

Article type
Research Article
Submitted
15 Feb 2019
Accepted
23 Mar 2019
First published
27 Mar 2019

Org. Chem. Front., 2019,6, 1577-1580

Palladium-catalyzed dearomative arylphosphorylation of indoles

J. Weng, L. Xing, W. Hou, R. Liang and Y. Jia, Org. Chem. Front., 2019, 6, 1577 DOI: 10.1039/C9QO00246D

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