Synthesis of Quinoline Derivatives by Multicomponent Reaction Using Niobium Pentachloride as Lewis Acid

2014 ◽  
Vol 52 (1) ◽  
pp. 273-277 ◽  
Author(s):  
Aloisio de Andrade ◽  
Giovanny Carvalho dos Santos ◽  
Luiz Carlos da Silva-Filho
ChemInform ◽  
2015 ◽  
Vol 46 (24) ◽  
pp. no-no
Author(s):  
Aloisio de Andrade ◽  
Giovanny Carvalho dos Santos ◽  
Luiz Carlos da Silva-Filho

2014 ◽  
Vol 50 (82) ◽  
pp. 12270-12272 ◽  
Author(s):  
V. P. Alex Raja ◽  
Giammarco Tenti ◽  
Subbu Perumal ◽  
J. Carlos Menéndez

Pyridines and fused pyridines are accessible by a combination of a Lewis acid-catalyzed multicomponent reaction and aromatization involving loss of a 2-furylmethyl chain.


Heterocycles ◽  
2007 ◽  
Vol 71 (3) ◽  
pp. 691 ◽  
Author(s):  
Kazuhiro Kobayashi ◽  
Yasutoshi Himei ◽  
Yuichi Izumi ◽  
Shuhei Fukamachi ◽  
Osamu Morikawa ◽  
...  

Synthesis ◽  
2017 ◽  
Vol 49 (11) ◽  
pp. 2402-2410 ◽  
Author(s):  
Willian dos Santos ◽  
Eliezer de Oliveira ◽  
Francisco Lavarda ◽  
Ives Leonarczyk ◽  
Marco Ferreira ◽  
...  

Phloroglucinol derivatives are an important class of natural compounds featuring the rhodomyrtone derivatives. In this work, the synthesis of compounds with a structure core of rhodomyrtosone I is described using a multicomponent reaction between aldehyde derivatives, dihydroresorcinol, and 3,5-dimethoxyphenol promoted by niobium pentachloride. This new method is simple, cost-effective, and provides a good yield. In addition, it can be conducted in good reaction times. Using Density Functional Theory (DFT) studies, bases are provided for a proposed reaction mechanism for the multicomponent reaction by exploring the energetics of proposed reactive intermediates and transition states.


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