Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1713
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dc.contributor.authorMahesh, S.-
dc.contributor.authorAnand, R.V.-
dc.contributor.authorPaluru, Dilip K.-
dc.contributor.authorAhmad, Feroz-
dc.contributor.authorPatil, Swati-
dc.contributor.authorKant, Guddi-
dc.date.accessioned2020-11-17T10:55:07Z-
dc.date.available2020-11-17T10:55:07Z-
dc.date.issued2017-
dc.identifier.citationAsian Journal of Organic Chemistry, 6(12)en_US
dc.identifier.other10.1002/ajoc.201700419-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/full/10.1002/ajoc.201700419-
dc.identifier.urihttp://hdl.handle.net/123456789/1713-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractA Cu‐catalyzed protocol for the synthesis of indolizine‐containing diaryl‐ and triarylmethane derivatives through a 5‐endo‐dig cyclization of 2‐(2‐enynyl)pyridines, followed by a remote addition of nucleophiles, such as hydride and 2‐naphthols, is described.en_US
dc.language.isoen_USen_US
dc.publisherWileyen_US
dc.subjectSynthesisen_US
dc.subject5‐endo‐dig cyclizationen_US
dc.subjectCu‐catalyzeden_US
dc.subjecthydride and 2‐naphtholsen_US
dc.titleSynthesis of Indolizine-Containing Diaryl- and Triarylmethanes through a Cu-Catalyzed Domino Cyclization of 2-(2-Enynyl)pyridinesen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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