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
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
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE