C-N and N-N bond formation via reductive cyclization: Progress in cadogan/cadogan-sundberg reaction

dc.contributor.authorKaur, M.
dc.contributor.authorKumar, Raj
dc.date.accessioned2018-08-24T03:50:21Z
dc.date.accessioned2024-08-13T12:06:21Z
dc.date.available2018-08-24T03:50:21Z
dc.date.available2024-08-13T12:06:21Z
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, onitrostyrenes 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 M. and Kumar Raj (2018) C?N and N?N bond formation via Reductive Cyclization: Progress in Cadogan /Cadogan?Sundberg Reaction?. Chemistry Select, 3(19), 5330-5340. 10.1002/slct.201800779en_US
dc.identifier.doi10.1002/slct.201800779
dc.identifier.issn23656549
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/1555
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/abs/10.1002/slct.201800779
dc.language.isoen_USen_US
dc.publisherWiley-Blackwellen_US
dc.subjectCadogan/cadogan-sundberg reactionen_US
dc.subjectCarbazoleen_US
dc.subjectIndazoleen_US
dc.subjectReductive cyclizationen_US
dc.subjectTrialkylphosphiteen_US
dc.titleC-N and N-N bond formation via reductive cyclization: Progress in cadogan/cadogan-sundberg reactionen_US
dc.title.journalChemistry Select
dc.typeArticleen_US

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