Studies on isocyanides and related compounds : a novel synthesis of pyrroles via Ugi reaction
- Author
- BOSSIO, R; MARCACCINI, S; PEPINO, R
CNR Univ. Firenze, cent. studio chimica struttura composti eterociclici applicazioni, dip. chimica organica Ugo Schiff, 50121 Firenze, Italy - Source
Synthesis (Stuttgart). 1994, Num 8, pp 765-766 ; ref : 7 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)
- Cycle 5 chaînons Enaminonitrile Enol éther Hétérocycle azote Lactame Méthylation Réaction Ugi Acétique acide(cyano) Acétophénone(2-arylamino) Cyclohexane(isocyano) Pyrrole-2-carboxylique acide(4-cyano-1,3-diaryl-2,5-dihydro-5-oxo) cyclohexylamide Pyrrole-2-carboxylique acide(4-cyano-1,3-diaryl-5-méthoxy) cyclohexylamide
- Keyword (en)
- Five membered ring Enaminonitrile Enol ether Nitrogen heterocycle Lactam Methylation Ugi reaction
- Keyword (es)
- Ciclo 5 eslabones Enaminonitrilo Enol eter Heterociclo nitrógeno Lactamo Metilación Reacción Ugi
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06B Heterocyclic compounds with only one n hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4170797
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-1994-25565 
https://dx.doi.org/10.1055/s-1994-25565
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