415678-24-9Relevant academic research and scientific papers
4-N-aryl(benzyl)amino-4-hetaryl-1-butenes as building blocks in heterocyclic synthesis. 1. New route to 4,6-dimethyl-2-pyridylquinolines from the 4-N-p-methylphenylamino-4-pyridyl-1-butenes
Vargas Mendez, Leonor Y.,Kouznetsov, Vladimir,Stashenko, Elena,Bahsas, Al,Amaro-Luis, Juan
, p. 323 - 326 (2001)
Mediated-acid intramolecular cyclisation of 4-N-p-methylphenylamino-4-pyridyl-1-butenes 4-6 was used to obtain new C-2 pyridyl substituted 4,6-dimethyl-1,2,3,4-tetrahydroquinolines 7-9, which were oxidised then to their aromatic analogues 10-12 in good yi
In vitro antifungal activity of new series of homoallylamines and related compounds with inhibitory properties of the synthesis of fungal cell wall polymers
Vargas M., Leonor Y.,Castelli, Maria V.,Kouznetsov, Vladimir V.,Urbina G., Juan M.,Lopez, Silvia N.,Sortino, Maximiliano,Enriz, Ricardo D.,Ribas, Juan C.,Zacchino, Susana
, p. 1531 - 1550 (2007/10/03)
The synthesis, in vitro antifungal evaluation and SAR studies of 101 compounds of the 4-aryl-, 4-alkyl-, 4-pyridyl or -quinolinyl-4-N-arylamino-1-butenes series and related compounds, are reported here. Active structures showed to inhibit (1,3)-β-D-glucan and mainly chitin synthases, enzymes that catalyze the synthesis of the major fungal cell wall polymers.
