Synthesis of p-aminobenzamides of aminopiperidazines as potential antiarrhythmic agents
- Author
- KORNET, M. J1 ; ABDUL-NABI ALI, K1 ; STEINBERG, M. I
[1] Univ. Kentucky, coll. pharmacy, div. medicinal chemistry pharmaceutics, Lexington KY 40536-0082, United States - Source
Journal of heterocyclic chemistry. 1994, Vol 31, Num 4, pp 967-971 ; ref : 9 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)
- Activité biologique Addition Diels Alder Aminoamide Antiarythmique Cycle 6 chaînons Hydrazine organique Hétérocycle azote Réduction chimique Benzamide(4-amino-N-[1,2-diméthyl-perhydropyridazin-4-yl]) Benzamide(4-amino-N-[2-(1,2,2-triméthylhydrazino)éthyl]) Benzamide(4-amino-[N-(2-[2-méthyl-perhydropyridazin-1-yl])]) Pyridazine(1-[2-aminoéthyl]-2-méthyl-perhydro) Pyridazine(4-amino-1,2-diméthyl-perhydro)
- Keyword (en)
- Biological activity Diels Alder addition Aminoamide Antiarrhythmia agent Six membered ring Organic hydrazine Nitrogen heterocycle Chemical reduction
- Keyword (es)
- Actividad biológica Adición Diels Alder Aminoamida Antiarrítmico Ciclo 6 eslabones Hidracina orgánica Heterociclo nitrógeno Reducción química
- 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
- 4215439
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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