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

Authors
Kim, Gyeong UnCho, HyunmiLee, Jae KyunLee, Jae YeolTae, JinsungMin, Sun-JoonKang, TaekCho, Yong Seo
Issue Date
Dec-2022
Publisher
Royal Society of Chemistry
Citation
Chemical Communications, v.59, no.1, pp 82 - 85
Pages
4
Indexed
SCIE
SCOPUS
Journal Title
Chemical Communications
Volume
59
Number
1
Start Page
82
End Page
85
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/111430
DOI
10.1039/d2cc05133h
ISSN
1359-7345
1364-548X
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.
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COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY > DEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING > 1. Journal Articles

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