PREPARATION AND SYNTHETIC APPLICATIONS OF IMINOPHOSPHORANES DERIVED FROM O-SUBSTITUTED ARYLAZIDES - PREPARATION OF PYRAZOLO[1,2-B]INDAZOLE,4H-3,1-BENZOXAZINE AND QUINOLINE DERIVATIVES - CRYSTAL-STRUCTURE OF 2-(4-METHOXYBENZOYLAMINO)PHENYL]-4-METHYLQUINOLINE
P. Molina et al., PREPARATION AND SYNTHETIC APPLICATIONS OF IMINOPHOSPHORANES DERIVED FROM O-SUBSTITUTED ARYLAZIDES - PREPARATION OF PYRAZOLO[1,2-B]INDAZOLE,4H-3,1-BENZOXAZINE AND QUINOLINE DERIVATIVES - CRYSTAL-STRUCTURE OF 2-(4-METHOXYBENZOYLAMINO)PHENYL]-4-METHYLQUINOLINE, Tetrahedron, 49(34), 1993, pp. 7599-7612
The Staudinger reaction of several ortho-substituted arylazides with t
riphenylphosphine has been studied. The reaction product is found to b
e strongly dependent on the nature of the ortho-substituent. The Aza W
ittig-type reaction of iminophosphorane derived from the ortho-azido a
cetophenone with isocyanates and aroyl chlorides leads to the previous
ly unreported 4-methylene-4H-3,1-benzoxazine ring. The crystal and mol
ecular structure of 2-(4-methoxybenzoylamino)phenyl]-4-methylquinoline
has been established by X-Ray diffraction methods.