Direct hydroxylation of indoles in superacids: application to the hydroxylation of tryptophan and tryptamine derivatives
- Author
- BERRIER, C1 ; JACQUESY, J. C; JOUANNETAUD, M. P; RENOUX, A
[1] Fac. sci., lab. chimie XII, Poitiers 86022, France - Source
New journal of chemistry (1987). 1987, Vol 11, Num 8-9, pp 611-615 ; ref : 19 ref
- CODEN
- NJCHE5
- ISSN
- 1144-0546
- Scientific domain
- Biochemistry, molecular biology, biophysics; Chemistry
- Publisher
- CNRS, Paris
/
Royal Society of Chemistry, Cambridge
- Publication country
- France
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aminoacide Composé aromatique Composé bicyclique Hydrogène Fluorure Hydrogène Peroxyde Hydroxylation Hétérocycle azote Phénols Spectre RMN Superacide Carbazole(tétrahydro-«1,2,3,4») Carbazolol-6(tétrahydro-«1,2,3,4») Hydrogène 1 Indole(méthyl-3) Indole(trifluoroacétamido-«2p» éthyl-«3») Indole Indolol-5(méthyl-«3») Stiborane(pentafluoro) Tryptophane(hydroxy-«5» «N»-trifluoroacétyl) ester méthyle Tryptophane(«N»-trifluoroacétyl) ester méthyle
- Keyword (en)
- Aminoacid Aromatic compound Bicyclic compound Hydrogen Fluorides Hydrogen Peroxides Hydroxylation Nitrogen heterocycle Phenols NMR spectrum Superacid
- Keyword (es)
- Aminoacido Compuesto aromatico Compuesto bicíclico Hidrógeno Hidrógeno Hidroxilacion Heterociclo nitrógeno Fenoles Espectro de RMN Superácido
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06B Heterocyclic compounds with only one n hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 8332875
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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