Formation of Five- and Six-Membered Heterocyclic Rings under Radical Cyclization Conditions
- Author
- MAJUMDAR, K. C1 2 ; KARUNAKAR, Galla V1 ; SINHA, Biswajit2
[1] Department of Chemical Sciences, Tezpur University, Napaam, Tezpur 784024, Assam, India
[2] Department of Chemistry, University of Kalyani, Kalyani 741235, India - Source
Synthesis (Stuttgart). 2012, Num 16, pp 2475-2505, 31 p ; ref : 120 ref
- CODEN
- SYNTBF
- ISSN
- 0039-7881
- Scientific domain
- Organic chemistry
- Publisher
- Thieme, Stuttgart
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Author keyword
- atom-transfer radical cyclization cascade cyclization nitrogen heterocycles oxidative radical cyclization radical cyclization radical relay cyclization tandem radical cyclization tributyltin hydride
- Keyword (fr)
- Cycle 6 chaînons Cyclisation Hétérocycle azote Molécule organique Oxydation Radical libre organique Réaction successive Réaction tandem Stannane(tributyl)
- Keyword (en)
- Six membered ring Cyclization Nitrogen heterocycle Organic molecule Oxidation Organic free radical Successive reaction Tandem reaction Tributylstannane
- Keyword (es)
- Ciclo 6 eslabones Ciclización Heterociclo nitrógeno Molécula orgánica Oxidación Radical libre orgánico Reacción consecutiva Reacción tándem
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03B Reactivity and mechanisms / 001C03B04 Free radicals chemistry
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 26212547
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1055/s-0032-1316566 
https://dx.doi.org/10.1055/s-0032-1316566
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