Issue 37, 2024

Anionic aza 8π-electrocyclization as an unprecedented pathway versus 7-endo-dig: DFT study on the mechanism of base-catalyzed benzofuroazepine synthesis via cyclization of (2-alkynylbenzyl)oxy nitriles

Abstract

DFT calculations are used to disclose the mechanism of Brønsted base-mediated cyclization of (2-alkynylbenzyl)oxy nitriles for the synthesis of benzofuroazepines. In 2015, the synthesis of substituted benzofuroazepines was reported by Zeni et al. via a stepwise mechanism known as 7-endo-dig. However, DFT calculations revealed that the anionic aza 8π-electrocyclization is more favorable than the proposed 7-endo-dig mechanism.

Graphical abstract: Anionic aza 8π-electrocyclization as an unprecedented pathway versus 7-endo-dig: DFT study on the mechanism of base-catalyzed benzofuroazepine synthesis via cyclization of (2-alkynylbenzyl)oxy nitriles

Supplementary files

Article information

Article type
Paper
Submitted
19 Jun 2024
Accepted
28 Aug 2024
First published
30 Aug 2024

Phys. Chem. Chem. Phys., 2024,26, 24431-24437

Anionic aza 8π-electrocyclization as an unprecedented pathway versus 7-endo-dig: DFT study on the mechanism of base-catalyzed benzofuroazepine synthesis via cyclization of (2-alkynylbenzyl)oxy nitriles

O. Amiri and A. Bazgir, Phys. Chem. Chem. Phys., 2024, 26, 24431 DOI: 10.1039/D4CP02458C

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