REACTION OF 5-ARYL-2-TOSYLMETHYLIMINO-2,3-DIHYDRO-3-FURANONES WITH SUBSTITUTED N-(BENZYLIDENE)BENZYLAMINES - CRYSTAL-STRUCTURE OF P-METHOXYPHENYL-2-(P-CHLOROBENZOYL)ACETYLIMIDAZOLE
Sn. Shurov et al., REACTION OF 5-ARYL-2-TOSYLMETHYLIMINO-2,3-DIHYDRO-3-FURANONES WITH SUBSTITUTED N-(BENZYLIDENE)BENZYLAMINES - CRYSTAL-STRUCTURE OF P-METHOXYPHENYL-2-(P-CHLOROBENZOYL)ACETYLIMIDAZOLE, Russian chemical bulletin, 44(10), 1995, pp. 1933-1936
5-Aryl-2-aroylacetyl-1-benzylimidazoles were synthesized by treatment
of 5-aryl-2-tosylmethylimino-2,3-dihydro-3-furanones with N-(benzylide
ne)benzylamines containing electron-donating substitutents in the benz
ylidene moiety. The structure of 1-benzyl-5-p-methoxyphenyl-2-(p-chlor
obenzoyl) acetylimidazole was studied by X-ray diffraction.