Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9097
Title: Metal- and Solvent-Free Approach to Diversely Substituted Picolinates via Domino Reaction of Cyclic Sulfamidate Imines with β,γ-Unsaturated α-Ketocarbonyls
Authors: Biswas, Soumen
Majee, Debashis
Guin, Soumitra
Samanta, Sampak
Keywords: Reaction kinetics;Synthesis (chemical);Aza-heterocycles;Domino reactions;Eco-friendly;Functionalized;Imidazo[1 ,2-a]pyridine;Metal solvent;Rapid construction;Solvent free;Solvents;1,4 diazabicyclo[2.2.2]octane;carbonyl derivative;heterocyclic compound;imidazo[ 1,2 a]pyridine;imine;metal;picolinic acid derivative;pyridine derivative;solvent;sulfamide derivative;unclassified drug;annulation reaction;Article;arylation;chemical structure;cyclization;drug synthesis;microwave irradiation;organic chemistry;substitution reaction
Issue Date: 2017
Publisher: American Chemical Society
Citation: Biswas, S., Majee, D., Guin, S., & Samanta, S. (2017). Metal- and solvent-free approach to diversely substituted picolinates via domino reaction of cyclic sulfamidate imines with β,γ-unsaturated α-ketocarbonyls. Journal of Organic Chemistry, 82(20), 10928-10938. doi:10.1021/acs.joc.7b01792
Abstract: An efficient, solvent-free, and eco-friendly domino reaction of 5/6-membered cyclic sulfamidate imines with a variety of β, γ-unsaturated α-ketocarbonyls in neat conditions under MW irradiation promoted by DABCO as a solid organobase has been developed for the rapid construction of a novel class of densely functionalized picolinates. This interesting metal-solvent-free tactic allows a wide range of useful functionalities on the aryl rings and delivers good to excellent yields of the aforesaid aza-heterocycles within short time spans (20-40 min). A biologically promising imidazo[1,2-a]pyridine was successfully synthesized through our unique procedure. © 2017 American Chemical Society.
URI: https://doi.org/10.1021/acs.joc.7b01792
https://dspace.iiti.ac.in/handle/123456789/9097
ISSN: 0022-3263
Type of Material: Journal Article
Appears in Collections:Department of Chemistry

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