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TEMPO-Mediated Polyyne Cyclization
DOI:10.1021/acs.orglett.5c00651.png)
Abstract
En 中文
In this work, we report the cyclization of sulfur-linked tetraynes under 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO) radical conditions, leading to the formation of novel pentadehydro-Diels-Alder-type addition products. Through this study, we expand the scope of radical-mediated cyclization reactions of polyyne compounds. The results offer new opportunities for the development of radical-based synthetic methodologies.
Keywords:
NITROXYL RADICALS
ARYNES
METAL
CHEMISTRY
OXIDATION
BENZYNE
CYCLOAROMATIZATION
SYSTEM
Journal
IF:
5
Papers:
3.9W
Citations:
10.0W
Organization
No organization information available

