Issue 37, 2024

Diastereoselective dearomative bifunctionalization of isoquinolinium salts to access bridged tetrahydroisoquinolines

Abstract

Herein, we report a diastereoselective dearomative bifunctionalization strategy of using isoquinolinium salts to access bridged tetrahydroisoquinolines. The strategy relies on the strategic use of allenes and amines as reaction partners to generate binucleophilic species in situ for subsequent dearomatization.

Graphical abstract: Diastereoselective dearomative bifunctionalization of isoquinolinium salts to access bridged tetrahydroisoquinolines

Supplementary files

Article information

Article type
Communication
Submitted
01 Jul 2024
Accepted
02 Sep 2024
First published
02 Sep 2024

New J. Chem., 2024,48, 16151-16154

Diastereoselective dearomative bifunctionalization of isoquinolinium salts to access bridged tetrahydroisoquinolines

J. Pei, T. Tang, J. Zhang, Y. Qin, P. Cheng and Q. Wang, New J. Chem., 2024, 48, 16151 DOI: 10.1039/D4NJ02968B

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