C‐N and N‐N bond formation via Reductive Cyclization: Progress in Cadogan /Cadogan‐Sundberg Reaction.

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dc.contributor.authorKaur, Manpreet
dc.contributor.authorKumar, Raj Kumar
dc.date.accessioned2019-03-26T09:06:58Z
dc.date.accessioned2024-08-13T12:06:35Z
dc.date.available2019-03-26T09:06:58Z
dc.date.available2024-08-13T12:06:35Z
dc.date.issued2018
dc.description.abstractCadogan/Cadogan‐Sundberg cyclization reaction has been reported as one of the most efficient routes for the synthesis of a wide variety of N‐heterocycles from the easily accessible starting materials such as o‐nitrobiaryls or o‐nitroarenes, o‐nitrostyrenes by treating with tetravalent phosphorus compounds (trialkyl or triaryl phosphines or trialkyl phosphites). The reaction has been successfully employed in Carbon‐Carbon as well as Carbon‐Nitrogen bond formation for the scaffolds like carbazole, indoles, coumarins, and indazoles. To the best of authors’ knowledge, the present review is the first compilation of the literature from almost two decades (2000 to present) on Cadogan/Cadogan‐Sundberg cyclization reaction, its scope, mechanistic aspects, and limitations.en_US
dc.identifier.citationKaur, Manpreeten_US
dc.identifier.citationKumar, Raj Kumar (2018) C‐N and N‐N bond formation via Reductive Cyclization: Progress in Cadogan /Cadogan‐Sundberg Reaction. ChemistrySelect. Vol. 3(19), PP.5330-5340. https://doi.org/10.1002/slct.201800779en_US
dc.identifier.doi10.1002/slct.201800779
dc.identifier.issnOnline- 2365-6549
dc.identifier.urihttp://10.2.3.109/handle/32116/2244
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/full/10.1002/slct.201800779
dc.language.isoenen_US
dc.publisherwileyen_US
dc.titleC‐N and N‐N bond formation via Reductive Cyclization: Progress in Cadogan /Cadogan‐Sundberg Reaction.en_US
dc.title.journalChemistrySelecten_US
dc.typeArticleen_US
dc.type.accesstypeClosed Accessen_US

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