57262-00-7Relevant articles and documents
Bi(OTf)3-catalyzed Friedl?nder hetero-annulation: A rapid synthesis of 2,3,4-trisubstituted quinolines
Yadav,Reddy,Premalatha
, p. 963 - 966 (2004)
Polysubstituted quinolines are readily prepared in high yields under extremely mild conditions through a sequential condensation/annulation reaction of 2-aminoaryl ketones and α-methylene ketones using a catalytic amount of bismuth triflate.
An efficient and green microwave-assisted synthesis of quinoline derivatives via knoevengal condensation
Tasqeeruddin, Syed,Asiri, Yahya,Alsherhri, Jaber Abdullah
supporting information, p. 157 - 163 (2020/02/04)
We have developed an efficient and green synthesis of quinoline derivatives using L-proline under Knoevenagel condensation. L-proline was found to be an efficient catalyst for the Knoevenagel condensation of substituted 2-aminoaryl ketones 1 with the acti
Highly efficient Br?nsted acid and Lewis acid catalysis systems for the Friedl?nder Quinoline synthesis
Zhou, Xiao-Yu,Chen, Xia,Wang, Liang-Guang
supporting information, p. 830 - 837 (2018/03/12)
The efficient and green Br?nsted acid or Lewis acid catalysis systems for the Friedl?nder synthesis of 2,3,4-trisubstituted quinolines from the condensation of 2-aminoarylketones and β-ketoesters/ketones had been developed. The results confirmed that 4-to
