Please use this identifier to cite or link to this item: http://10.9.150.37:8080/dspace//handle/atmiyauni/861
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dc.contributor.authorRathod, Chirag H.-
dc.contributor.authorPatel, Anilkumar S.-
dc.date.accessioned2023-05-08T03:09:58Z-
dc.date.available2023-05-08T03:09:58Z-
dc.date.issued2021-
dc.identifier.citationRathod, C. H., & Patel, A. S. (2021). Synthesis of Pyrrole Derivatives via Cycloaddition Reaction of Reissert Hydrofluoroborate Salts with α-Bromoacrylamides. Analytical Chemistry Letters, 11(3), 289-302.en_US
dc.identifier.issn2230-7532-
dc.identifier.urihttp://10.9.150.37:8080/dspace//handle/atmiyauni/861-
dc.descriptionAuthors are thankful to the School of Science, RK University & Faculty of Science, Atmiya University, Rajkot for providing a laboratory experiment facility. We also thank to the Central Instrumental facility (CIF), Shree M. & N. Virani Science College (Autonomous) for providing spectral analysis.en_US
dc.description.abstractAn investigation of α-bromoacrylamide as a dienophile for the cycloaddition reaction of Reissert hydrofluoroborate salt of quinoline/phenanthridine has been carried out. The optimized condition has been developed for the [4+2] cycloaddition reaction of Reissert hydrofluroborate salt and a-bromoacrylamide by using K2 CO3 in DMF under moderate temperature to afford highly functionalized pyrrole derivatives (6a-f and 7a-f) in very good to excellent yield. The structures of newly synthesized compounds were established based on FT-IR, Mass, 1 H and 13C NMR spectral techniques. Besides, the structure of compound 7a has been confirmed by 2D NMR experiments (COSY and HSQC).en_US
dc.language.isoenen_US
dc.publisherAnalytical Chemistry Letters, Taylor & Francisen_US
dc.subjectReissert hydrofluoroborate salten_US
dc.subjectPyrrole derivativesen_US
dc.subjectCycloaddition reactionen_US
dc.subjectα-Bromoacrylamidesen_US
dc.titleSynthesis of pyrrole derivatives via cycloaddition reaction of reissert hydrofluoroborate salts with α-bromoacrylamidesen_US
dc.typeArticleen_US
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