Abstract
An efficient ultrasonic synthesis of structurally diverse Pyridine-2,6-dithiazole/ dioxazole analogues were designed and achieved by ultrasonic irradiation techniqueas well as by conventional method. The advantages of this eco-friendly ultrasonic irradiation method over conventional method are excellent yields, no metal catalyst, less toxic solvents, simple workup, no chromatographic column purifications. The precursor S-6 and S-16 and their Schiff base derivatives S-10 to S-15 and S-17 to S-22 were characterized by spectral means, found consistent for expected structure. To check their biological potential molecular docking and invitro antimicrobial studies were also performed.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call