Efficient construction of 3-arylquinolin-4(1H)-ones via in situ Meinwald rearrangement/intramolecular reductive cyclization of 2′-nitrochalcone epoxides
An efficient method for construction of 3-arylquinolin-4(1H)-ones via in situ Meinwald rearrangement/intramolecular reductive cyclization of 2′-nitrochalcone epoxides has been developed. The practical approach is of excellent functional groups compatibili
Wang, Sheng,Zhao, Chao,Liu, Ting,Yu, Lifang,Yang, Fan,Tang, Jie
p. 7025 - 7031
(2016/10/14)
Antitubercular Agents : Part III - Synthesis of Substituted 2-Arylisatogens
A number of 2-arylisatogens (VII) have been prepared starting from o-nitroacetophenones (I).Condensation of I with different aromatic aldehydes (II) gives the corresponding o-nitrochalkones (III) which on epoxidation followed by treatment with BF3-etherat
Sahasrabudhe, A. B.,Kamath, H. V.,Bapat, B. V.,Kulkarni, Sheshgiri N.
p. 230 - 232
(2007/10/02)
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