ELECTROCHEMICAL SYNTHESIS AND X-RAY MOLECULAR-STRUCTURE OF 3,4,5-TRIARYL-2-ARYLIMINOOXAZOLINES

Authors
GUIRADO A ZAPATA A JONES PG
Citation
A. Guirado et al., ELECTROCHEMICAL SYNTHESIS AND X-RAY MOLECULAR-STRUCTURE OF 3,4,5-TRIARYL-2-ARYLIMINOOXAZOLINES, Tetrahedron, 51(37), 1995, pp. 10375-10384
Citations number
20
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron → ACNP
ISSN journal
00404020
Volume
51
Issue
37
Year of publication
1995
Pages
10375 - 10384
Database
ISI
SICI code
0040-4020(1995)51:37<10375:ESAXMO>2.0.ZU;2-I
Abstract
Selective cathodic reduction of benzilmonoimines in aprotic medium at a mercury pool cathode, under constant potential, in the presence of e quimolecular amounts of N-arylcarbonimidoyl dichlorides, provides a ne w and very convenient method for the synthesis of 3,4,5-triaryl-2-aryl iminooxazolines. Geometrical characteristics of this little known clas s of heterocycle were determined by X-ray crystallography of henylimin o)-5-(4-methoxyphenyl)-4-phenyloxazoline.