Journal of medicinal chemistry, 28(11), 1558-1564 (1985-11-01)
A series of novel arylfluoroquinolones has been prepared. These derivatives are characterized by having a fluorine atom at the 6-position, substituted amino groups at the 7-position, and substituted phenyl groups at the 1-position. Structure-activity relationship (SAR) studies indicate that the
Eco-friendly synthesis of fluorine-containing pyrazoline derivatives over potassium carbonate.
Patel VM and Desai KR.
ARKIVOC (Gainesville, FL, United States), 1, 123-129 (2004)
Farmaco (Societa chimica italiana : 1989), 56(8), 565-570 (2001-10-17)
A series of 7-arylidene-6-(2,4-dichloro-5-fluorophenyl)-3-substituted-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines (3) were prepared by the condensation of 4-amino-5-mercapto-3-substituted-1,2,4-triazoles (1) and 3-aryl-1-(2,4-dichloro-5-fluorophenyl)-2-bromo-2-propen-1-one (2). An alternative route for the synthesis of the title compound 3 has been described. The newly synthesised compounds were characterised on the basis of