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
- 2023-01
- Publisher
- Royal Society of Chemistry
- Citation
- Chemical Communications, v.59, no.1, pp.82 - 85
- 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.
- Keywords
- MEDIUM-SIZED RINGS; SCAFFOLD; DIKETOPIPERAZINE; HETEROCYCLES; DERIVATIVES; DIVERSITY
- ISSN
- 1359-7345
- URI
- https://pubs.kist.re.kr/handle/201004/114170
- DOI
- 10.1039/d2cc05133h
- Appears in Collections:
- KIST Article > 2023
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