New one-step general synthesis of 2,3-dihydronaphtho[2,3-b]furan-4,9-diones by regioselective photoaddition of 2-hydroxy-1,4-naphthoquinones with various alkenes and its application to a two-step synthesis of maturinone
- Author
- KOBAYASHI, K; SHIMIZU, H; SASAKI, A; SUGINOME, H
Hokkaido univ., fac. eng., organic synthesis div., Sapporo 060, Japan - Source
Journal of organic chemistry. 1991, Vol 56, Num 10, pp 3204-3205, 2 p ; ref : 13 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)
- Composé aromatique Composé tricyclique Composé éthylénique Hétérocycle oxygène Photoaddition Phénols Quinone Régiosélectivité Isobutène Naphto [2,3-b] furane-«4,9»-dione(«2,2»-diméthyl-«2,3,4,9»-tétrahydro) «1,4»-Naphtoquinone(«2»-hydroxy)
- Keyword (en)
- Aromatic compound Tricyclic compound Ethylenic compound Oxygen heterocycle Photoaddition Phenols Quinone Regioselectivity
- Keyword (es)
- Compuesto aromático Compuesto tricíclico Compuesto etilénico Heterociclo oxígeno Fotoadición Fenoles Quinona Regioselectividad
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06A Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 19639449
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/jo00010a003 
https://dx.doi.org/10.1021/jo00010a003
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