ChemInform Abstract: Access to N-Thioalkenyl and N-(o-Thio)aryl-benzimidazol-2-ones by Ring Opening of Thiazolobenzimidazolium and Benzimidazobenzothiazolium Salts and C-O Bond Cleavage of an Alkoxide
Autor: | Fabien Coppola, Daniel Farran, Federico Andreoli, Nicolas Vanthuyne, Radia Kaid-Slimane, Christian Roussel |
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Rok vydání: | 2015 |
Předmět: | |
Zdroj: | ChemInform. 46 |
ISSN: | 0931-7597 |
Popis: | We report herein the synthesis of highly functionalized 1,3-dihydro-2H-benzimidazol-2-ones via a ring opening of thiazolo[3,2-a]benzimidazolium or benzimidazo[2,1-b][1,3]benzothiazol-6-ium salts and an unusual C-O bond cleavage of an alkoxide. A large variety of benzimidazolones bearing an original N-thioalkenyl or N-(o-thio)aryl group was obtained in high yields. The developed chemistry provides efficient and rapid access to the privileged benzimidazol-2-one scaffold. |
Databáze: | OpenAIRE |
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