Reductive phenolic coupling: A novel intramolecular capture of a nitro-intermediate generated through reduction of a nitrobenzophenone

Autor:	Abdul Jabbar, Zsussanna Rozsa, Alexander R. Forrester, R. Alan Howie, John R. Lewis, Shaikh S. Nizami, Kalman Szendrei
Rok vydání:	1992
Předmět:	Ethanol Bicyclic molecule Chemistry Organic Chemistry chemistry.chemical_element Crystal structure Zinc Biochemistry Combinatorial chemistry chemistry.chemical_compound Intramolecular force Drug Discovery Nitro Molecule Organic chemistry Amine gas treating
Zdroj:	Tetrahedron Letters. 33:4645-4648
ISSN:	0040-4039
Popis:	Zinc ethanol reduction of 2′-nitro-2,6-dimethoxy-4-hydroxybenzophenone gives the amine together with a spiro-hydroxylamine - the result of a novel reductive phenolic coupling process.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::ad83c9d20a374eca7b8df7cf9a626372 https://doi.org/10.1016/s0040-4039(00)61335-7 Zobrazit plný text záznamu