Cyclic meso-ionic heterocycles. Part 24. The reaction of 1,2-dithiolium-4-olates with aniline. The formationof 11-phenylbenz[b]indeno[2,1-e]-1,4-thiazine
摘要:
Reaction of the type B meso-ionic heterocycle 3,5-diphenyl-1,2-dithiolium-4-olate (1) with aniline yields N-phenyl-(3-phenyl-1-phenylimino-inden-2-yl)-amine (10) and 11-phenylbenz[b]indeno[2,1-e]-1,4-thiazine (12). Mechanistic investigations establish that the 3-phenylindenylamine (10) is an intermediate in the formation of the tetracyclic 1,4-thiazine (12).
Cyclic meso-ionic heterocycles. Part 24. The reaction of 1,2-dithiolium-4-olates with aniline. The formationof 11-phenylbenz[b]indeno[2,1-e]-1,4-thiazine
摘要:
Reaction of the type B meso-ionic heterocycle 3,5-diphenyl-1,2-dithiolium-4-olate (1) with aniline yields N-phenyl-(3-phenyl-1-phenylimino-inden-2-yl)-amine (10) and 11-phenylbenz[b]indeno[2,1-e]-1,4-thiazine (12). Mechanistic investigations establish that the 3-phenylindenylamine (10) is an intermediate in the formation of the tetracyclic 1,4-thiazine (12).
McKinnon, David M.; Clark, Peter D.; Martin, Robert O., Canadian Journal of Chemistry, 1987, vol. 65, p. 2830 - 2833
作者:McKinnon, David M.、Clark, Peter D.、Martin, Robert O.、Delbaere, Louis T.J.、Quail, J.Wilson
DOI:——
日期:——
Cyclic meso-ionic heterocycles. Part 24. The reaction of 1,2-dithiolium-4-olates with aniline. The formationof 11-phenylbenz[b]indeno[2,1-e]-1,4-thiazine
作者:Christopher G. Newton、W.David Ollis、Graham P. Rowson、Margaret J. Hamor、Thomas A. Hamor
DOI:10.1016/s0040-4020(01)80482-8
日期:1992.1
Reaction of the type B meso-ionic heterocycle 3,5-diphenyl-1,2-dithiolium-4-olate (1) with aniline yields N-phenyl-(3-phenyl-1-phenylimino-inden-2-yl)-amine (10) and 11-phenylbenz[b]indeno[2,1-e]-1,4-thiazine (12). Mechanistic investigations establish that the 3-phenylindenylamine (10) is an intermediate in the formation of the tetracyclic 1,4-thiazine (12).