Studies with polyfunctionality substituted heteroaromatics: arylhydrazononitriles for the synthesis of polyfunctionally substituted azines
- Author
- MOHAMED HILMY ELNAGDI1 ; AHMED HAFEZ HUSSIEN ELGHANDOUR1 ; ABDEL FATTAH ALI HARB; ABDEL HALEEM MOSTAFA HUSSIEN1 ; SAOUD ABDEL MENIEM METWALLY
[1] Cairo univ., fac. sci., dep. chemistry, Giza, Egypt - Source
Heterocycles (Sendai). 1994, Vol 38, Num 4, pp 739-750 ; ref : 11 ref
- CODEN
- HTCYAM
- ISSN
- 0385-5414
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Amidine Cycle 5 chaînons Cycle 6 chaînons Cyclisation Dinitrile Hydrazone Hétérocycle azote Nitrile Réactivité chimique 1,2,3-Triazol-4-carbonitrile(5-phényloxy) 2,2p-Méthylènedimidazol-4-one(α-phénylhydrazono-4,4p,5,5p-tétrahydro) Malononitrile(arylhydrazono) Pyrimidine-2-acétonitrile(6-amino-4-aryloxy-5-phényldiazényl-α-phénylhydrazono)
- Keyword (en)
- Amidine Five membered ring Six membered ring Cyclization Dinitrile Hydrazone Nitrogen heterocycle Nitrile Chemical reactivity
- Keyword (es)
- Amidina Ciclo 5 eslabones Ciclo 6 eslabones Ciclización Dinitrilo Hidrazona Heterociclo nitrógeno Nitrilo Reactividad 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
- 3996931
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-92-6057 
https://dx.doi.org/10.3987/COM-92-6057
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