The synthesis of 7,9-dimethoxy-5,11-dimethyl-6H-pyrido-[4,3-b]carbazole (7,9-dimethoxyellipticine) via a regioselective bromination and some bromination and ipso substitution reactions of the 2,4-dimethoxycarbazole system
- Author
- HALL, R. J; SHANNON, P. V. R; OLIVEIRA-CAMPOS, A. M. F; QUEIROZ, M. J. R. P
Univ. Wales coll. Cardiff, school chemistry applied chemistry, Cardiff CF1 3TB, United Kingdom - Source
Journal of chemical research. Synopses (Print). 1992, Num 1, pp 2-3 ; ref : 6 ref
- CODEN
- JRPSDC
- ISSN
- 0308-2342
- Scientific domain
- Organic chemistry; Atomic molecular physics
- Publisher
- Turpin, Letchworth
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Attaque ipso Bromation Composé aromatique Composé tricyclique Composé tétracyclique Hétérocycle azote Régiosélectivité Carbazole(1-bromo-2,4-diméthoxy) Ellipticine(7,9-diméthoxy) Indolo isoquinoléine dérivé
- Keyword (en)
- Ipso attack Bromination Aromatic compound Tricyclic compound Tetracyclic compound Nitrogen heterocycle Regioselectivity
- Keyword (es)
- Ataque ipso Bromuración Compuesto aromático Compuesto tricíclico Compuesto tetracíclico Heterociclo nitrógeno Regioselectividad
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06C Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5111938
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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