81829-63-2Relevant academic research and scientific papers
Synthesis of novel 2-aryloxy-3-(4-chlorophenyl)-8-substituted-5-aryl-8,9-dihydro-3H-chromeno[2,3-d]pyrimidine-4,6(5H,7H)-dione derivatives
Wang, Zhong-Xia,Chen, Li-Zhuang,Wang, Fang-Ming,Li, Bei,Han, Guang-Fan
, p. 744 - 750 (2015)
Twenty-one novel 2-aryloxy-3-(4-chlorophenyl)-8-substituted-5-aryl-8,9-dihydro-3H-chromeno[2,3-d]pyrimidine-4,6(5H,7H)-diones 5a, 5b, 5c, 5d, 5e, 5f, 5g, 5h, 5i, 5j, 5k, 5l, 5m, 5n, 5o, 5p, 5q, 5r, 5s, 5t, 5u were designed and easily synthesized via a tan
CYCLIZATION OF NITRILES. XX. SYNTHESIS OF CONDENSED 2-AMINO-4H-PYRANS AND THE MOLECULAR STRUCTURE OF 2-AMINO-7,7-DIMETHYL-4-(3-FLUOROPHENYL)-5-OXO-3-ETHOXYCARBONYL-5,6,7,8-TETRAHYDRO-4H-BENZOPYRAN
Sharanina, L. G.,Nesterov, V. N.,Klokol, G. V.,Rodinovskaya, L. A.,Shklover, V. E.,et al.
, p. 1185 - 1191 (2007/10/02)
2-Amino-5,6,7,8-tetrahydro-4H-benzopyrans were obtained by the reaction of 1,3-cyclohexanedione and its substituted derivatives with the arylidene derivatives of malononitrile and ethyl cyanoacetate.The crystal structure of 2-amino-7,7-dimethyl-4-(3-fl
CYCLIZATION REACTIONS OF NITRILES. REACTION OF ARYLIDENEMALONONITRILES WITH 1,3-DICARBONYL COMPOUNDS
Sharanin, Yu. A.,Promonenkov, V. K.,Sharanina, L. G.
, p. 544 - 548 (2007/10/02)
The reaction of 1,3-dicarbonyl compounds with arylidene derivatives of malononitrile and ethyl cyanoacetate leads to the formation of substituted 2-amino-4H-pyrans.In the case of 1,1,1-trifluoro-3-(2-thenoyl)acetone acid cleavage of the Michael adduct occurs, and this leads to 2-aryl-3-(2-thenoyl)-1,1-dicyanopropanes. 1,3-Indanedione reacts by exchange of the methylene components and gives the corresponding 2-arylidene-1,3-indanediones.
