Preparation of naturally occurring anthraquinones using the aryne reaction
- Author
- HE ZHAO; BIEHL, E
Southern Methodist univ., dep. chemistry, Dallas TX 75275, United States - Source
Journal of natural products (Print). 1995, Vol 58, Num 12, pp 1970-1974 ; ref : 13 ref
- CODEN
- JNPRDF
- ISSN
- 0163-3864
- Scientific domain
- Pharmacology drugs
- Publisher
- American Chemical Society, Washington, DC
/
American Society of Pharmacognosy, Glendale, AZ
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Anthracène dérivé Anthraquinone dérivé Aryne Composé benzénique condensé Composé tricyclique Déméthylation Ether Lithiation Phénols Quinone Synthèse chimique Anthraquinone(1,3-diméthoxy-2-méthyl) Anthraquinone(3-hydroxy-1-méthoxy-2-méthyl) Anthraquinone(3-hydroxy-2-hydroxyméthyl-1-méthoxy) Benzène(1-bromo-2,4-diméthoxy-3-méthyl) Isobenzofurane dérivé Phtalide Rubiadine
- Keyword (en)
- Anthracene derivatives Anthraquinone derivatives Aryne Condensed benzenic compound Tricyclic compound Demethylation Ether Lithiation Phenols Quinone Chemical synthesis
- Keyword (es)
- Antraceno derivado Antraquinona derivado Arino Compuesto bencénico condensado Compuesto tricíclico Desmetilación Eter Litiación Fenoles Quinona 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
- 2995327
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/np50126a031 
https://dx.doi.org/10.1021/np50126a031
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