Cu‐Catalyzed Hydrophosphonylation of 2‐(2‐Enynyl)pyridines: Easy Access to Indolizine‐Containing Diarylmethylphosphonates

dc.contributor.authorMahesh, S.
dc.contributor.authorAnand, R.V.
dc.date.accessioned2020-12-04T06:32:04Z
dc.date.available2020-12-04T06:32:04Z
dc.date.issued2017
dc.description.abstractAn efficient protocol for the synthesis of indolizine‐containing unsymmetrical diarylmethylphosphonates through a Cu‐catalyzed 5‐endo‐dig ring‐closing reaction of 2‐(2‐enynyl)pyridines followed by remote hydrophosphonylation is described. A competent method for the synthesis of indolizine‐based diarylmethylphosphonates is described. This protocol involves a metal‐catalyzed 5‐endo‐dig‐cyclization of 2‐(2‐enynyl)pyridine derivatives followed by a remote addition of diarylphosphites to provide indolizine‐containing diarylmethylphosphonates in good yields.en_US
dc.identifier.citationEuropean Journal of Organic Chemistry, 2017(19), pp.2698-2706.en_US
dc.identifier.otherhttps://doi.org/10.1002/ejoc.201700146
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.201700146
dc.identifier.urihttp://hdl.handle.net/123456789/2662
dc.language.isoenen_US
dc.publisherWILEY‐VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.subjectHydrophosphonylationen_US
dc.subjectNitrogen heterocyclesen_US
dc.subjectCyclizationen_US
dc.titleCu‐Catalyzed Hydrophosphonylation of 2‐(2‐Enynyl)pyridines: Easy Access to Indolizine‐Containing Diarylmethylphosphonatesen_US
dc.typeArticleen_US

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