Issue 9, 2022

Assembly of tetracyclic tetrahydrocarbazoles via a visible-light promoted cascade process

Abstract

We disclose an efficient method for the synthesis of tetracyclic tetrahydrocarbazoles via a visible-light promoted cascade reaction of alkene tethered indoles and bromodifluoroacetate esters. This reaction involves the formation of two C–C bonds and one C–N bond and proceeds via a key reactive tetrahydrocarbazole intermediate and dual cyclization. The reaction features mild conditions, wide substrate scope, and good chemical yields, and provides a new strategy for the synthesis of tetracyclic tetrahydrocarbazole derivatives. The synthetic utility of this reaction was further demonstrated by the large-scale synthesis and reduction of the obtained tetracyclic tetrahydrocarbazole product.

Graphical abstract: Assembly of tetracyclic tetrahydrocarbazoles via a visible-light promoted cascade process

Supplementary files

Article information

Article type
Research Article
Submitted
14 Feb 2022
Accepted
21 Mar 2022
First published
23 Mar 2022

Org. Chem. Front., 2022,9, 2516-2521

Assembly of tetracyclic tetrahydrocarbazoles via a visible-light promoted cascade process

H. Mei, Y. Yu, C. Wang, A. Liu and J. Han, Org. Chem. Front., 2022, 9, 2516 DOI: 10.1039/D2QO00247G

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