Synthesis of substituted pyrido[3,2-b]indoles (δ-carbolines)
- Author
- MEROUR, J.-Y; MEROUR, A
CNRS Univ. Orléans, lab. chimie bioorganique analytique, 45067 Orléans, France - Source
Synthesis (Stuttgart). 1994, Num 8, pp 767-769 ; ref : 19 ref
- CODEN
- SYNTBF
- ISSN
- 0039-7881
- Scientific domain
- Organic chemistry
- Publisher
- Thieme, New York, NY
/
Thieme, Stuttgart
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Keyword (fr)
- Addition Diels Alder Aminolyse Carboxamide Composé aromatique Composé tricyclique Enaminone Enol éther Hétérocycle azote Inversion polarité Réaction catalytique Ytterbium Ether(éthyl vinyl) Indol-3-one(1-acétyl-2-arylidène-2,3-dihydro) Pyrano[3,2-b]indole dérivé Pyrido[3,2-b]indole dérivé
- Keyword (en)
- Diels Alder addition Aminolysis Carboxamide Aromatic compound Tricyclic compound Enaminone Enol ether Nitrogen heterocycle Polarity inversion Catalytic reaction Ytterbium
- Keyword (es)
- Adición Diels Alder Aminolisis Carboxamida Compuesto aromático Compuesto tricíclico Enaminona Enol eter Heterociclo nitrógeno Inversión polaridad Reacción catalítica Yterbio
- 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
- 4170798
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
10.1055/s-1994-25566 
https://dx.doi.org/10.1055/s-1994-25566
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