90543-03-6Relevant articles and documents
Chemistry of iminofurans: X. Synthesis and hydrolysis of 5-aryl(hetaryl)-2-[(4,5,6,7-tetrahydro-1-benzothiophen-2-yl)imino]furan-3(2H)-ones
Panchenko,Shipilovskikh,Rubtsov
, p. 343 - 348 (2016/06/06)
5-Aryl(hetaryl)furan-2,3-diones reacted with N-(triphenyl-λ5-phosphanylidene)-4,5,6,7-tetrahydro-1-benzothiophen-2-amines to give 5-aryl(hetaryl)-2-[(4,5,6,7-tetrahydro-1-benzothiophen-2-yl)imino]furan-3(2H)-ones whose acid hydrolysis afforded 4-aryl(hetaryl)-2-hydroxy-4-oxo-N-(4,5,6,7-tetrahydro-1-benzothiophen- 2-yl)but-2-enamides.
Heterocyclic β-Enamino Esters, 31 Novel 6:7-, 6:8-, and 5:6:7-Combinations of Heterocondensed Pyrimidines from Iminophosphoranes of Heterocyclic β-Enamino Esters. - Stable Heterocyclic Ylides
Wamhoff, Heinrich,Haffmanns, Guenter
, p. 585 - 621 (2007/10/02)
With acetylenic esters the (5-azolylimino)triphenylphosphoranes 10a-d do not show any cycloaddition tendency, while the (2-thienylimino)triphenylphosphoranes 8a,b yield the stable ylids 13a,b.By treatment with phenyl isocyanate the iminophosphoranes 16a-m