Diastereoselective dearomative bifunctionalization of isoquinolinium salts to access bridged tetrahydroisoquinolines

Abstract

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

Supplementary files

Article information

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

New J. Chem., 2024, Accepted Manuscript

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, Accepted Manuscript , DOI: 10.1039/D4NJ02968B

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