5-Hydroxy-2 H -pyrrol-2-ones and not 2-aminofurans are the cycloaddition products between alkyl isocyanides and benzyliden-1,3-diketones

Autor:	Simona Dossena, Ugo Vendrame, Maurizio Mondoni, Sara Frattini, Enzo Cereda, Monica Quai
Rok vydání:	2004
Předmět:	chemistry.chemical_classification chemistry Organic Chemistry Drug Discovery Organic chemistry Biochemistry Cycloaddition Alkyl
Zdroj:	Tetrahedron Letters. 45:1413-1416
ISSN:	0040-4039
DOI:	10.1016/j.tetlet.2003.12.059
Popis:	New insights into the cycloaddition reaction between alkyl isocyanides and benzyliden-1,3-diketones are reported. 5-Hydroxy-N-substituted-2H-pyrrol-2-ones and not substituted furans, as previously reported, are formed. The proof of the structure relies on a thorough analytical investigation and X-ray crystallography.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::b6347f318fc3cafcac81d8a639a3fe87 https://doi.org/10.1016/j.tetlet.2003.12.059 Zobrazit plný text záznamu Full Text from ScienceDirect