79429-63-3Relevant academic research and scientific papers
Synthesis of chromeno[2,3-b ]indol-11(6 H)-one via PhI(OAc)2-mediated intramolecular oxidative C(sp2)-N(H2) bond formation
Sun, Jiyun,Zhang-Negrerie, Daisy,Du, Yunfei,Zhao, Kang
, p. 1200 - 1206 (2015)
Various chromeno[2,3-b]indol-11(6H)-ones were conveniently constructed via phenyliodine(III) diacetate (PIDA)-mediated intramolecular oxidative annulation. This method, while realizing a direct oxidative C-N bond formation between an aromatic ring and a p
Flavones and structurally related 4-chromenones inhibit carbonic anhydrases by a different mechanism of action compared to coumarins
Balboni, Gianfranco,Congiu, Cenzo,Onnis, Valentina,Maresca, Alfonso,Scozzafava, Andrea,Winum, Jean-Yves,Maietti, Annalisa,Supuran, Claudiu T.
experimental part, p. 3063 - 3066 (2012/06/17)
An inhibition study of several carbonic anhydrase (CA, EC 4.2.1.1) isoforms with flavones and aminoflavones, compounds possessing a rather similar scaffold with the coumarins, recently discovered inhibitors of this enzyme, is reported. The natural product
Convenient synthesis of chromones and quinolinones
Hemavathi,Naveen,Lokanatha Rai
, p. 409 - 410 (2013/09/24)
A one pot synthesis of substituted chromones and quinolinones by condensing commercially available and cheaper molecules like salicylic acid and anthranilic acid respectively with alkenes / nitriles followed by insitu cyclization using ammonium acetate as base has been achieved.
