84186-24-3Relevant articles and documents
An affordable DABCO-based ionic liquid efficiency in the synthesis of 3-amino-1-aryl-1H-benzo[f] chromene-2-carbonitrile, 1-(benzothiazolylamino)phenylmethyl-2-naphthol, and 1-(benzoimidazolylamino)phenylmethyl-2-naphthol derivatives
Nabinia, Nazanin,Shirini, Farhad,Tajik, Hassan,Mashhadinezhad, Maryam,Langarudi, Mohaddeseh Safarpoor Nikoo
, p. 2147 - 2157 (2018/08/03)
In this study, [H2-DABCO][HSO4]2 is applied as an acidic ionic liquid to exclude some disadvantages of former methods reported for the synthesis of 3-amino-1-aryl-1H-benzo[f]chromene-2-carbonitrile, 1-(benzothiazolylamino)
CYCLIZATION OF NITRILES. XXIII. ADDITION OF ACTIVE PHENOLS TO ELECTRON-DEFICIENT ETHYLENES, ACCOMPANIED BY CYCLIZAION TO 2-AMINO-4H-BENZOPYRANS. CRYSTAL STRUCTURE OF 2-AMINO-4-(2-FLUOROPHENYL)-3-ETHOXYCARBONYL-4H-NAPHTHOPYRAN
Klokol, G.V.,Sharanina, L.G.,Nesterov, V.N.,Shklover, V.E.,Sharanin, Yu.A.,Struchkov, Yu.T.
, p. 369 - 377 (2007/10/02)
Active phenols and also 2-naphthol react with arylidene derivatives of malononitrile and cyanoacetic ester with the formation of the corresponding substituted 2-amino-4H-benzo- and 2-amino-4H-naphthopyrans.By X-ray crystallographic investigation