7509-45-7Relevant academic research and scientific papers
One-pot and catalyst-free synthesis of pyrroloquinolinediones and quinolinedicarboxylates
Zhang, Xiaofeng,Dhawan, Gagan,Muthengi, Alex,Liu, Shuai,Wang, Wei,Legris, Marc,Zhang, Wei
supporting information, p. 3851 - 3855 (2017/08/22)
A method for the catalyst-free synthesis of pyrroloquinolinediones and quinolinedicarboxylates is developed through a one-pot synthesis involving denitrogenation of azide, benzisoxazole formation, aza-Diels-Alder cycloaddition, and dehydrative aromatization. Only stoichiometric amounts of N2 and H2O are produced as by-products. A comprehensive green chemistry metrics analysis indicated that this method is much more efficient and greener than two reported methods for the synthesis of pyrroloquinolinediones.
Cyclic hydrazides 1. Synthesis of 4-hydroxy-1-oxo-1,2-dihydropyridazino[4,5-b]quinolines
Rozhkov,Piskunova,Gol'd,Kalvin'sh
, p. 77 - 91 (2007/10/03)
A series of dimethyl esters and cyclic hydrazides of quinoline-2,3-dicarboxylic acid has been synthesized with different substituents in the benzene ring.
