Articles written in Journal of Chemical Sciences
Volume 126 Issue 1 January 2014 pp 117-125
An expeditious neat procedure was developed for the synthesis of a series of new methyl phenyl heterocyclic phosphinates (
Volume 128 Issue 8 August 2016 pp 1303-1313 Regular Article
An efficient, environmentally benign and green method was developed for the synthesis of α-aminophosphonates by one-pot three-component reaction (Kabachnik-Fields reaction) of amine (4-(4-chlorophenoxy) aniline), aldehydes and diethyl phosphite using catalyst, SiO₂-ZnBr₂ under solvent-free conditions. The developed method under conventional conditions was further optimized in microwave and ultrasonication methods. A series of α-aminophosphonates, diethyl (4-(4-chlorophenoxy) phenylamino)(aryl/ heteroaryl) methylphosphonates was synthesized to check the generality. The catalyst, SiO₂-ZnBr₂ afforded good yields of products in all the methods in the range of 85–97% but variation was observed in reaction time. Microwave irradiation method took very less time (4–8 min) as compared with ultrasonication (35–52 min) and conventional (2–3 h) conditions. The major advantages are simple and mild conditions, short reaction times, high yield of the product with purity, use of cheap catalyst and reusability of the catalyst until to three times without significant loss of activity. Antibacterial and antifungal activities were evaluated for the title compounds (50 and 100μg/mL) including minimum inhibitory concentrations. A few of the newly synthesized α-aminophosphonates exhibited promising antimicrobial activity at lower MIC values in the range of 15.0–25.0μg/mL and closer to the standards (5–12μg/mL).
Volume 134, 2022
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