Syntheses of indolyl-4(3H)-quinazolinones
- Author
- HERMECZ, I1 ; KÖKÖSI, J; PODANYI, B1 ; SZASZ, G
[1] Chinoin Pharmaceutical & Chemical Works ltd, 1325 Budapest, Hungary - Source
Heterocycles (Sendai). 1994, Vol 37, Num 2, pp 903-914 ; ref : 30 ref
- CODEN
- HTCYAM
- ISSN
- 0385-5414
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Catalyse acide Composé aromatique Composé bicyclique Cyclisation Hydrazone Hétérocycle azote Lactame Réaction intramoléculaire Indole-2-carboxylique acide(3-[3,4-dihydro-2-méthyl-4-oxoquinazolin-2-yl]) ester méthyle Quinazolin-4-one(3,4-dihydr-2-[indol-2-yl]) Quinazolin-4-one(3,4-dihydro-2-[1-(N-méthylanilino)éthyl]) Quinazolin-4-one(3,4-dihydro-2-[2-(phénylhydrazono)éthyl]) Quinazolin-4-one(3,4-dihydro-3-[1,2-diméthylindol-3-yl]) Quinazoline-2-propionique acide(3,4-dihydro-3-méthyl-4-oxo-β-phénylhydrazono) ester éthyle
- Keyword (en)
- Acid catalysis Aromatic compound Bicyclic compound Cyclization Hydrazone Nitrogen heterocycle Lactam Intramolecular reaction
- Keyword (es)
- Catálisis ácida Compuesto aromático Compuesto bicíclico Ciclización Hidrazona Heterociclo nitrógeno Lactamo Reacción intramolecular
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06C Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 3949441
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
10.3987/COM-93-S83 
https://dx.doi.org/10.3987/COM-93-S83
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