210686-76-3Relevant academic research and scientific papers
Studies on the alkylation of quinolin-2(1H)-one derivatives
Chen, Chia-Ling,Chen, I-Li,Chen, Jih-Jung,Wei, Dau-Chang,Hsieh, Han-Jie,Chang, Ken-Ming,Tzeng, Cherng-Chyi,Wang, Tai-Chi
, p. 2812 - 2816 (2015/06/02)
Alkylation of quinolin-2(1H)-one (1) and its C(6) and C(7) substituted dervatives (OMe, OBn, and Cl) with 2-bromoacetophenone or chloroacetone under basic condition (K2CO3 in DMF) gave a mixture of N1- and O2- a
Synthesis of dibenzo[a,f]quinolizinium and 2-phenyloxazolo[3,2-a]quinolinium perchlorates via acid-catalyzed cyclization of 1-(2-oxo-2-Phenylethyl)quinolin-2(1h)-ones
Chen, I-Li,Chen, Yeh-Long,Wang, Tai-Chi,Tzeng, Cherng-Chyi
, p. 131 - 141 (2007/10/03)
Treatment of certain N-alkylated quinolin-2(1H)-ones with concentrated H2SO4 afforded oxazolo[3,2-a]quinolin-10-ylium perchlorates via a Z-form enol intermediate while others gave dibenzo[a,f]quinolizinium perchlorates via an E-form
α-Methylidene-γ-butyrolactones: Synthesis and Evaluation of Quinolin-2(1H)-one Derivatives
Wang, Tai-Chi,Chen, Yeh-Long,Tzeng, Cherng-Chyi,Liou, Shorong-Shii,Tzeng, Weng-Feng,Chang, Ya-Ling,Teng, Che-Ming
, p. 1038 - 1047 (2007/10/03)
As a continuation of our previous studies on the synthesis and antiplatelet activity of quinolin-2(1H)-ones with an α-methylidene-γ-butyrolactone substituted at O(8), the O(6)- and N(1)-substituted isomers were synthesized and evaluated for antiplatelet a
