Synthesis of polycyclic aromatics and heteroaromatics via electrophilic cyclization
- Author
- TUANLI YAO1 ; CAMPO, Marino A1 ; LAROCK, Richard C1
[1] Department of Chemistry, Iowa State University, Ames, Iowa 50011, United States - Source
Journal of organic chemistry. 2005, Vol 70, Num 9, pp 3511-3517, 7 p ; ref : 34 ref
- CODEN
- JOCEAH
- ISSN
- 0022-3263
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Biphényle dérivé Composé acétylénique Composé aromatique polycyclique Composé aromatique Condition opératoire modérée Cyclisation Groupe fonctionnel Hétérocycle Iode chlorure Phénanthrène dérivé Réaction électrophile Succinimide(N-bromo) Synthèse chimique
- Keyword (en)
- Biphenyl derivatives Acetylenic compound Polycyclic aromatic compound Aromatic compound Mild operating conditions Cyclization Functional group Heterocyclic compound Iodine chlorides Phenanthrene derivatives Electrophilic reaction N-Bromosuccinimide Chemical synthesis
- Keyword (es)
- Bifenilo derivado Compuesto acetilénico Compuesto aromático policíclico Compuesto aromático Condición operatoria moderada Ciclización Grupo funcional Heterociclo Fenantreno derivado Reacción electrófila Síntesis química
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C04 Condensed benzenic and aromatic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 16723621
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
10.1021/jo050104y 
https://dx.doi.org/10.1021/jo050104y
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