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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Biswas, Soumen | en_US |
dc.contributor.author | Majee, Debashis | en_US |
dc.contributor.author | Guin, Soumitra | en_US |
dc.contributor.author | Samanta, Sampak | en_US |
dc.date.accessioned | 2022-03-17T01:00:00Z | - |
dc.date.accessioned | 2022-03-21T11:31:02Z | - |
dc.date.available | 2022-03-17T01:00:00Z | - |
dc.date.available | 2022-03-21T11:31:02Z | - |
dc.date.issued | 2017 | - |
dc.identifier.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 | en_US |
dc.identifier.issn | 0022-3263 | - |
dc.identifier.other | EID(2-s2.0-85031897450) | - |
dc.identifier.uri | https://doi.org/10.1021/acs.joc.7b01792 | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/9097 | - |
dc.description.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. | en_US |
dc.language.iso | en | en_US |
dc.publisher | American Chemical Society | en_US |
dc.source | Journal of Organic Chemistry | en_US |
dc.subject | Reaction kinetics | en_US |
dc.subject | Synthesis (chemical) | en_US |
dc.subject | Aza-heterocycles | en_US |
dc.subject | Domino reactions | en_US |
dc.subject | Eco-friendly | en_US |
dc.subject | Functionalized | en_US |
dc.subject | Imidazo[1 ,2-a]pyridine | en_US |
dc.subject | Metal solvent | en_US |
dc.subject | Rapid construction | en_US |
dc.subject | Solvent free | en_US |
dc.subject | Solvents | en_US |
dc.subject | 1,4 diazabicyclo[2.2.2]octane | en_US |
dc.subject | carbonyl derivative | en_US |
dc.subject | heterocyclic compound | en_US |
dc.subject | imidazo[ 1,2 a]pyridine | en_US |
dc.subject | imine | en_US |
dc.subject | metal | en_US |
dc.subject | picolinic acid derivative | en_US |
dc.subject | pyridine derivative | en_US |
dc.subject | solvent | en_US |
dc.subject | sulfamide derivative | en_US |
dc.subject | unclassified drug | en_US |
dc.subject | annulation reaction | en_US |
dc.subject | Article | en_US |
dc.subject | arylation | en_US |
dc.subject | chemical structure | en_US |
dc.subject | cyclization | en_US |
dc.subject | drug synthesis | en_US |
dc.subject | microwave irradiation | en_US |
dc.subject | organic chemistry | en_US |
dc.subject | substitution reaction | en_US |
dc.title | Metal- and Solvent-Free Approach to Diversely Substituted Picolinates via Domino Reaction of Cyclic Sulfamidate Imines with β,γ-Unsaturated α-Ketocarbonyls | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Chemistry |
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