Efficient Strategy for the Synthesis of 4-Hydroxy-1H-pyrrole-2,3-dicarboxylic Ester Derivatives Using Transition-Metal-Oxide Catalysts

Autor:	A. Chandra Shekhar, V. Luke Paul, T. Yakaiah, A. Raghuram Reddy, P. Shanthan Rao, Banda Narsaiah
Rok vydání:	2010
Předmět:	chemistry.chemical_compound Annulation Acetylene chemistry Transition metal Organic Chemistry Oxide Organic chemistry Ring (chemistry) Ceric ammonium nitrate Catalysis Pyrrole
Zdroj:	Synthetic Communications. 40:3152-3158
ISSN:	1532-2432 0039-7911
DOI:	10.1080/00397910903370675
Popis:	A facile and an efficient strategy for the synthesis of multisubstituted pyrrole derivatives was developed using an unusual ring annulation of dialkyl acetylene dicarboxylic ester and α-amino acids with transition-metal oxides such as mercuric(II) oxide and silver(I) oxide and complexes such as ceric ammonium nitrate (CAN) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDCI) as catalysts.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::61e7c047db21b08a5698eccd1f945148 https://doi.org/10.1080/00397910903370675 Zobrazit plný text záznamu Plný text ve formátu PDF Plný text ve formátu HTML
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