Issue 1, 2023

Stereoselective synthesis of 1,6-diazecanes by a tandem aza-Prins type dimerization and cyclization process

Abstract

We report the stereocontrolled synthesis of 1,6-diazecanes via a tandem aza-Prins type reaction of N-acyliminium ions with allylsilanes. It involves an aza-Prins type dimerization and cyclization in a single-step operation. This reaction represents the first example of 10-membered N-heterocycle synthesis using an aza-Prins reaction. Also, the interesting formation of an unusual tetracyclic compound through further cyclization of 1,6-diazecane and bicyclic compounds by the intramolecular cyclization of linear allylsilane are described. This tandem aza-Prins protocol provides a new synthetic strategy for the direct synthesis of medium-sized nitrogen heterocycles.

Graphical abstract: Stereoselective synthesis of 1,6-diazecanes by a tandem aza-Prins type dimerization and cyclization process

Supplementary files

Article information

Article type
Communication
Submitted
17 Sep 2022
Accepted
30 Nov 2022
First published
30 Nov 2022

Chem. Commun., 2023,59, 82-85

Stereoselective synthesis of 1,6-diazecanes by a tandem aza-Prins type dimerization and cyclization process

G. U. Kim, H. Cho, J. K. Lee, J. Y. Lee, J. Tae, S. Min, T. Kang and Y. S. Cho, Chem. Commun., 2023, 59, 82 DOI: 10.1039/D2CC05133H

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