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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 | Samanta, Sampak | en_US |
dc.date.accessioned | 2022-03-17T01:00:00Z | - |
dc.date.accessioned | 2022-03-21T11:32:42Z | - |
dc.date.available | 2022-03-17T01:00:00Z | - |
dc.date.available | 2022-03-21T11:32:42Z | - |
dc.date.issued | 2014 | - |
dc.identifier.citation | Biswas, S., Majee, D., Dagar, A., & Samanta, S. (2014). Metal-free one-pot protocol for the preparation of unexpected carbazole derivative in water: Easy access to pyrimidocarbazole and pyridocarbazolone derivatives. Synlett, 25(15), 2115-2120. doi:10.1055/s-0034-1378446 | en_US |
dc.identifier.issn | 0936-5214 | - |
dc.identifier.other | EID(2-s2.0-84904845216) | - |
dc.identifier.uri | https://doi.org/10.1055/s-0034-1378446 | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/9384 | - |
dc.description.abstract | A novel, one-pot, metal-free-based catalytic system for the synthesis of a series of functionalized 1-methoxycarbonyl-2-aryl/alkyl-9H-carbazole derivatives has been successfully achieved in water medium by the combination of methyl 2-(3-formyl-1H-indol-2-yl)acetate with aryl/alkyl-substituted β-acroleins using DABCO (20 mol%), followed by treatment of HCl under air at heating conditions. This sequential one-pot protocol provides moderate to good yields (51-68%) of aforesaid compounds. In addition, biologically important carbazole-fused new heterocyclic scaffolds can be synthesized through our procedure. © Georg Thieme Verlag Stuttgart, New York. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Georg Thieme Verlag | en_US |
dc.source | Synlett | en_US |
dc.subject | carbazole derivative | en_US |
dc.subject | pyridocarbazole derivative | en_US |
dc.subject | pyrimidocarbazole derivative | en_US |
dc.subject | unclassified drug | en_US |
dc.subject | alkylation | en_US |
dc.subject | aromatization | en_US |
dc.subject | article | en_US |
dc.subject | carbon nuclear magnetic resonance | en_US |
dc.subject | catalysis | en_US |
dc.subject | chemical bond | en_US |
dc.subject | chemical reaction | en_US |
dc.subject | chemical structure | en_US |
dc.subject | cyclization | en_US |
dc.subject | oxidative coupling | en_US |
dc.subject | proton nuclear magnetic resonance | en_US |
dc.subject | proton transport | en_US |
dc.subject | stoichiometry | en_US |
dc.subject | synthesis | en_US |
dc.subject | tautomerization | en_US |
dc.title | Metal-free one-pot protocol for the preparation of unexpected carbazole derivative in water: Easy access to pyrimidocarbazole and pyridocarbazolone derivatives | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Chemistry |
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