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Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9100
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dc.contributor.authorRaghuvanshi, Abhinaven_US
dc.contributor.authorSingh, Amrendra Kumaren_US
dc.contributor.authorMobin, Shaikh M.en_US
dc.contributor.authorMathur, Pradeepen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:31:03Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:31:03Z-
dc.date.issued2017-
dc.identifier.citationRaghuvanshi, A., Singh, A. K., Mobin, S. M., & Mathur, P. (2017). Fe(CO)5 catalyzed [2+2+1] cycloaddition of alkyne, carbodiimide and CO for the synthesis of 5-iminopyrrolones. ChemistrySelect, 2(29), 9245-9248. doi:10.1002/slct.201701625en_US
dc.identifier.issn2365-6549-
dc.identifier.otherEID(2-s2.0-85041945667)-
dc.identifier.urihttps://doi.org/10.1002/slct.201701625-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9100-
dc.description.abstractUnder photolytic conditions, mixture of a terminal alkyne, a carbodiimide and CO, in presence of Fe(CO)5, undergoes [2+2+1] cocyclization to form 5-iminopyrrolone. Its formation has been shown to occur via a stable tetracarbonyl(2-aryl/alkyl maleoyl)iron intermediate. Addition of carbodiimide to the intermediate leads to the formation of 5-iminopyrrolone. This work highlights the role of Fe(CO)5 as a catalyst. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.language.isoenen_US
dc.publisherWiley-Blackwellen_US
dc.sourceChemistrySelecten_US
dc.titleFe(CO)5 Catalyzed [2+2+1] Cycloaddition of Alkyne, Carbodiimide and CO for the Synthesis of 5-Iminopyrrolonesen_US
dc.typeJournal Articleen_US
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