Synthesis and stereochemistry of new trihydrodiazabicyclo-[3.m.n]alkano[4',5':1,2]pyrido[3,4-b]indole ring system [1]
- Author
- MISZTAL, S; PALUCHOWSKA, M. H
Polish acad. sci., inst. pharmacology, dep. medicinal chemistry, 31343 Kralów, Poland - Source
Journal of heterocyclic chemistry. 1993, Vol 30, Num 6, pp 1543-1548
- CODEN
- JHTCAD
- ISSN
- 0022-152X
- Scientific domain
- Organic chemistry
- Publisher
- HeteroCorporation, Odessa, FL
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acylation Composé aromatique Composé pentacyclique Conformation Cyclisation Effet Overhauser Hétérocycle azote angulaire Lactame Méthode MNDO Réaction Pictet Spengler Structure moléculaire Ethano-1,4-diazépino[1',7':1,2]pyrido[3,4-b]indole dérivé Indole(3-[2-aminoéthyl]) Méthano diazépine pyrido indole dérivé Pipéridinone(1-benzyl) Pyrrolidin-3-one(1-benzyl) Spiro[pipéridine-4:1p-pyrido[4,3-b]indole] Spiro[pyrido[4,3-b]indole-1:3p-pyrrolidine]
- Keyword (en)
- Acylation Aromatic compound Pentacyclic compound Conformation Cyclization Overhauser effect Angular nitrogen heterocycle Lactam MNDO method Pictet Spengler reaction Molecular structure
- Keyword (es)
- Acilación Compuesto aromático Compuesto pentacíclico Conformación Ciclización Efecto Overhauser Heterociclo nitrógeno angular Lactamo Método MNDO Reacción Pictet Spengler Estructura molecular
- 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
- 3881839
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.5570300616 
https://dx.doi.org/10.1002/jhet.5570300616
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