Photocyclization reactions. II: Synthesis of dihydrobenzofuranols using photocyclization of ethyl 2-formylphenoxyacetates and ethyl 2-acetylphenoxyacetates
- Author
- HORAGUCHI, T1 ; TSUKADA, C; HASEGAWA, E; HASEGAWA, E; SHIMIZU, T; SUZUKI, T; TANEMURA, K
[1] Niigata univ., fac. sci., dep. chemistry, Ikarashi, Niigata 950-21, Japan - Source
Journal of heterocyclic chemistry. 1991, Vol 28, Num 5, pp 1273-1280 ; ref : 6 ref
- CODEN
- JHTCAD
- ISSN
- 0022-152X
- Scientific domain
- Organic chemistry
- Publisher
- HeteroCorporation, Odessa, FL
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aldéhyde Composé aromatique Composé bicyclique Cyclisation Cétoéther Effet substituant Ether Hétérocycle oxygène Réaction photochimique Acétique acide (2p-acétylphénoxy) ester éthyle Acétique acide (2p-formylphénoxy) ester éthyle Benzofurane-2-carboxylique acide (2,3-dihydro-3-hydroxy-3-méthyl) ester éthyle Benzofurane-2-carboxylique acide (2,3-dihydro-3â-hydroxy) ester éthyle
- Keyword (en)
- Aldehyde Aromatic compound Bicyclic compound Cyclization Ketoether Substituent effect Ether Oxygen heterocycle Photochemical reaction
- Keyword (es)
- Aldehído Compuesto aromático Compuesto bicíclico Ciclización Cetoéter Efecto sustituyente Eter Heterociclo oxígeno Reacción fotoquímica
- 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
- 5013381
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
10.1002/jhet.5570280519 
https://dx.doi.org/10.1002/jhet.5570280519
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