Diastereoselective synthesis of benzazocines by Zn(OTf)2-catalyzed (4+4) cyclocondensation of multisubstituted donor–acceptor cyclopropanes with anthranils

Abstract

A Zn(OTf)2-catalyzed (4+4) cyclocondensation of anthranils with 2-(trans-1-aroyl-2-arylcyclopropyl)malonates delivers a range of polycyclic benzazocines featuring an oxa-bridged eight-membered ring in excellent yields and with exclusive diastereoselectivity. Further synthetic manipulations of these products enable rapid access to diverse useful heterocyclic molecular scaffolds.

Graphical abstract: Diastereoselective synthesis of benzazocines by Zn(OTf)2-catalyzed (4+4) cyclocondensation of multisubstituted donor–acceptor cyclopropanes with anthranils

Supplementary files

Article information

Article type
Communication
Submitted
23 Dec 2024
Accepted
31 Jan 2025
First published
03 Feb 2025

Chem. Commun., 2025, Advance Article

Diastereoselective synthesis of benzazocines by Zn(OTf)2-catalyzed (4+4) cyclocondensation of multisubstituted donor–acceptor cyclopropanes with anthranils

X. Huang, G. Yang and Z. Chai, Chem. Commun., 2025, Advance Article , DOI: 10.1039/D4CC06690A

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