
Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/2662
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DC Field | Value | Language |
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dc.contributor.author | Mahesh, S. | - |
dc.contributor.author | Anand, R.V. | - |
dc.date.accessioned | 2020-12-04T06:32:04Z | - |
dc.date.available | 2020-12-04T06:32:04Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | European Journal of Organic Chemistry, 2017(19), pp.2698-2706. | en_US |
dc.identifier.other | https://doi.org/10.1002/ejoc.201700146 | - |
dc.identifier.uri | https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.201700146 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/2662 | - |
dc.description.abstract | An 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.language.iso | en | en_US |
dc.publisher | WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim | en_US |
dc.subject | Hydrophosphonylation | en_US |
dc.subject | Nitrogen heterocycles | en_US |
dc.subject | Cyclization | en_US |
dc.title | Cu‐Catalyzed Hydrophosphonylation of 2‐(2‐Enynyl)pyridines: Easy Access to Indolizine‐Containing Diarylmethylphosphonates | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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