Synthesis of 3-vinylpyrrole
- Author
- SETTAMBOLO, R; LAZZARONI, R; MESSERI, T; MAZZETTI, M; SALVADORI, P
CNR, ist. chimica quantistica energetica molecolare, dep. chimica industriale, 56126 Pisa, Italy - Source
Journal of organic chemistry. 1993, Vol 58, Num 27, pp 7899-7902 ; ref : 13 ref
- CODEN
- JOCEAH
- ISSN
- 0022-3263
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acylation Composé éthylénique Cycle 5 chaînons Déprotection Déshydratation Hétérocycle azote Pyrrole Réduction chimique Acide alcanoïque chlorure Pyrrole(3-[alc-1-ényl]) Pyrrole(3-acyl-1-tosyl) p-Toluènesulfonique acide chlorure
- Keyword (en)
- Acylation Ethylenic compound Five membered ring Deprotection Dehydration Nitrogen heterocycle Pyrrole Chemical reduction
- Keyword (es)
- Acilación Compuesto etilénico Ciclo 5 eslabones Desprotección Deshidratación Heterociclo nitrógeno Pirrol Reducción química
- 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
- 3869959
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
10.1021/jo00079a040 
https://dx.doi.org/10.1021/jo00079a040
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