期刊
ORGANIC CHEMISTRY FRONTIERS
卷 4, 期 7, 页码 1358-1362出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7qo00136c
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资金
- Ministry of Science and Technology of Taiwan
An efficient one pot synthesis of benzimidazole-fused isoindoles from 2-arylbenzimidazole and readily available conjugated alkenes has been explored. The developed domino strategy involved the ruthenium-catalyzed formation of two distinct C-C and C-N bonds and one new five-membered ring to afford a polycyclic molecule. The rapid and base-free reaction conditions and the broader substrate scope are salient features of this novel protocol. The ruthenium-catalyzed tandem reaction provides a direct tool for the easy and rapid access to a new benzoimidazoisoindole scaffold.
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