Synthesis and structural elucidation of novel quaternary pyridinium salt and indolizine derivatives as an anti-tubercular agent: In Silico and In Vitro screening
The in vitro anti-mycobacterial activity of a novel series of diversely substituted quaternary
pyridinium salts (3a-m) and indolizines (5a-h) were assessed against H37Rv strain of …
pyridinium salts (3a-m) and indolizines (5a-h) were assessed against H37Rv strain of …
Larvicidal activity, molecular docking, and molecular dynamics studies of 7-(trifluoromethyl)indolizine derivatives against Anopheles arabiensis
A novel series of 7-(trifluoromethyl) indolizine derivatives (4a-4n) was synthesized using a 1,
3-Dipolar cycloaddition reaction. Structure elucidation of the synthesized compounds was …
3-Dipolar cycloaddition reaction. Structure elucidation of the synthesized compounds was …
Tandem Knoevenagel‐Aldol Cyclization Towards Di and Trisubstituted Pyridines: Use of Malonaldehyde and Diethyl Malonate for the Synthesis of Indolizine
ST Dorai… - European Journal of …, 2024 - Wiley Online Library
An effective method for the construction of a multi‐functionalized pyridine motif of indolizine
using the [4+ 2] annulation pathway involves tandem Knoevenagel‐aldol cyclization as a …
using the [4+ 2] annulation pathway involves tandem Knoevenagel‐aldol cyclization as a …