Synthesis, antimicrobial activities and cytogenetic studies of newer diazepino quinoline derivatives via Vilsmeier–Haack reaction
R Nandhakumar, T Suresh, ALC Jude…
Index: Nandhakumar; Suresh; Jude, A.L. Calistus; Rajesh kannan; Mohan European Journal of Medicinal Chemistry, 2007 , vol. 42, # 8 p. 1128 - 1136
Full Text: HTML
Citation Number: 33
Abstract
The study of the Vilsmeier–Haack reagent on 4-hydroxyquinaldines resulted in a new versatile intermediate 4-chloro-3-formyl-2-(2-hydroxy-ethene-1-yl) quinolines, which on further treatment with hydrazine hydrate yielded the desired diazepino quinoline derivatives. All the synthesized diazepino quinoline derivatives are screened for their antibacterial and antifungal activities. Cytogenetic analysis of the samples is also reported.
Related Articles:
559. Quinaldine and 4-hydroxyquinaldine derivatives from m-chloroaniline and m-toluidine
[Spivey; Curd Journal of the Chemical Society, 1949 , p. 2656,2660]
559. Quinaldine and 4-hydroxyquinaldine derivatives from m-chloroaniline and m-toluidine
[Spivey; Curd Journal of the Chemical Society, 1949 , p. 2656,2660]