26190-82-9Relevant articles and documents
Photocatalytic Synthesis of Quinolines via Povarov Reaction under Oxidant-Free Conditions
Su, Long-Long,Zheng, Yi-Wen,Wang, Wen-Guang,Chen, Bin,Wei, Xiang-Zhu,Wu, Li-Zhu,Tung, Chen-Ho
supporting information, p. 1180 - 1185 (2022/02/14)
We describe here an approach for synthesizing quinolines either from N-alkyl anilines or from anilines and aldehydes. A dual-catalyst system consisting of a photocatalyst and a proton reduction cocatalyst is employed. Without the use of any sacrificial ox
Fe(CrO2)2-catalyzed, photoactivated oxidative one-pot tandem synthesis of substituted quinolines from primary alcohols and arylamines
Makhmutov, Aynur R.,Mustafin, Akhat G.,Usmanov, Salavat M.
, p. 369 - 374 (2018/05/28)
[Figure not available: see fulltext.] A one-pot tandem synthesis of substituted quinolines involving selective catalytic oxidation of primary alcohols to the corresponding aldehydes and their subsequent condensation with arylamines has been developed. Fe(CrO2)2 has been used as a catalyst, and oxidation has been performed with aqueous H2O2. To accelerate the catalytic oxidation of alcohols, photoactivation method has been applied.
Doebner-miller synthesis in a two-phase system: Practical preparation of quinolines
Matsugi,Tabusa,Minamikawa
, p. 8523 - 8525 (2007/10/03)
Doebner-Miller cyclization was carried out in a two-phase solvent system. The method has shown to be advantageous to the yield and to the ease of the work-up process. (C) 2000 Elsevier Science Ltd.
