Stereoselective synthesis of 1,6-diazecanes by a tandem aza-Prins type dimerization and cyclization process
- Authors
- Kim, Gyeong Un; Cho, Hyunmi; Lee, Jae Kyun; Lee, Jae Yeol; Tae, Jinsung; Min, Sun-Joon; Kang, Taek; Cho, 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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Collections - COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY > DEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING > 1. Journal Articles

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