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Title: | Metal-free one-pot protocol for the preparation of unexpected carbazole derivative in water: Easy access to pyrimidocarbazole and pyridocarbazolone derivatives |
Authors: | Biswas, Soumen Majee, Debashis Samanta, Sampak |
Keywords: | carbazole derivative;pyridocarbazole derivative;pyrimidocarbazole derivative;unclassified drug;alkylation;aromatization;article;carbon nuclear magnetic resonance;catalysis;chemical bond;chemical reaction;chemical structure;cyclization;oxidative coupling;proton nuclear magnetic resonance;proton transport;stoichiometry;synthesis;tautomerization |
Issue Date: | 2014 |
Publisher: | Georg Thieme Verlag |
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 |
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. |
URI: | https://doi.org/10.1055/s-0034-1378446 https://dspace.iiti.ac.in/handle/123456789/9384 |
ISSN: | 0936-5214 |
Type of Material: | Journal Article |
Appears in Collections: | Department of Chemistry |
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