Synthesis of N-Heterocycles by Reductive Cyclization of Nitro Compounds using Formate Esters as Carbon Monoxide Surrogates
Articolo
Data di Pubblicazione:
2018
Citazione:
Synthesis of N-Heterocycles by Reductive Cyclization of Nitro Compounds using Formate Esters as Carbon Monoxide Surrogates / D. Formenti, F. Ferretti, F. Ragaini. - In: CHEMCATCHEM. - ISSN 1867-3880. - 10:1(2018 Jan 09), pp. 148-152. [10.1002/cctc.201701214]
Abstract:
A series of alkyl and aryl formate esters were evaluated as CO sources in the Pd- and Pd/Ru-catalyzed reductive cyclization of substituted nitro compounds to afford heterocycles, especially indoles. Phenyl formate was found to be the most effective, and it allowed the desired products to be obtained in excellent yields, often higher than those previously reported with pressurized CO. Through detailed experiments and kinetic studies, we were able to discern between metal-catalyzed and base-mediated activation of phenyl formate and confirmed that just the base was effective in catalyzing its decarbonylation.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
amination; carbon monoxide surrogates; cyclization; nitrogen heterocycles; palladium; Catalysis; Physical and Theoretical Chemistry; Organic Chemistry; Inorganic Chemistry
Elenco autori:
D. Formenti, F. Ferretti, F. Ragaini
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