Synthesis of 3-alkylcoumarins and 3-alkyl-α,β-unsaturated δ-lactones from 3-diethylphosphonocoumarins, 3-diethylphosphonolactones and aldehydes
- Author
- FALSONE, G; CATENI, F; DE NARDO, M. M; DARAI, M. M
Univ. Trieste, dep. pharmaceutical sci., 34127 Trieste, Italy - Source
Zeitschrift für Naturforschung. B, A journal of chemical sciences. 1993, Vol 48, Num 10, pp 1391-1397 ; ref : 10 ref
- CODEN
- ZNBSEN
- ISSN
- 0932-0776
- Scientific domain
- Chemistry; Crystallography; Atomic molecular physics
- Publisher
- Verlag der Zeitschrift für Naturforschung, Tübingen
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Keyword (fr)
- Alkylation Composé aromatique Composé bicyclique Condensation Knoevenagel Coumarine dérivé Hétérocycle oxygène Lactone Réaction catalytique Réduction chimique 1-Benzopyran-2-one(3-arylméthyl) 1-Benzopyran-2-one(3-diéthoxyphosphoryl) Arènecarbaldéhyde Indoline-2,3-dione Pyran-2-one(3-diéthoxyphosphoryl-5,5-diméthyl-perhydro) Pyran-2-one(5,6-dihydro-5,5-diméthyl-3-[2-oxoindolin-3-yl])
- Keyword (en)
- Alkylation Aromatic compound Bicyclic compound Knoevenagel condensation Coumarine derivatives Oxygen heterocycle Lactone Catalytic reaction Chemical reduction
- Keyword (es)
- Alquilación Compuesto aromático Compuesto bicíclico Condensación Knoevenage Heterociclo oxígeno Lactona Reacción catalítica Reducción química
- 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
- 3856005
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
10.1515/znb-1993-1014 
https://dx.doi.org/10.1515/znb-1993-1014
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