62492-57-3Relevant academic research and scientific papers
Bakers' yeast-catalyzed reductive cleavage of 3-aryl-2,1-benzisoxazoles and its quaternary salts: An efficient green synthesis of 2-aminobenzophenones
Lekhok, Kushal C.,Prajapati, Dipak,Boruah, Ramesh C.,Mazumder, Sharbani,Borah, Tarun C.
experimental part, p. 1183 - 1187 (2011/10/01)
3-Aryl-2,1-benzisoxazoles and its salts underwent reductive cleavage of the N-O bond leading to 2-aminobenzophenones with bakers' yeast under non-fermenting conditions in aqueous media. The procedure gives excellent yields of 2-alkylamino- and 2-aminobenzophenones.
4,1-benzoxazepin derivatives and their use
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, (2008/06/13)
N-containing, condensed heterocyclic compounds and salts thereof are disclosed which are useful for inhibiting squalene synthetase and fungal growth, and which are useful for treating or preventing hyperlipidemia. Also disclosed is a method for producing
The Synthesis of Benzofuroquinolines. VIII. Some Halobenzofuroquinoline Derivatives
Yamaguchi, Seiji,Yokoi, Takashi,Yamada, Minoru,Arai, Hitomi,Uchiuzo, Yasuto,Kawase, Yoshiyuki
, p. 1003 - 1005 (2007/10/02)
Three 2-halo-6(5H)-benzofuroquinolinones 1 (X = F, Cl, Br) were synthesized in two procedures, photocyclization of N-benzyl-N-(p-halophenyl)-2-benzofurancarboxamides 3 (X = F, Cl, Br) and condensation of 2-amino-2'-hydroxybenzophenones 7 (X = F, Cl
