Synthesis and tautomeric equilibrium of 6-amino-5-benzyl-3-methylpyrazin-2-one. An acceptor-donor-donor nucleoside base analog
- Author
- VOEGEL, J. J; VON KROSIGK, U; BENNER, S. A
ETH Zürich, lab. organic chemistry, 8092 Zürich, Switzerland - Source
Journal of organic chemistry. 1993, Vol 58, Num 26, pp 7542-7547 ; ref : 47 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)
- Composé modèle Constante équilibre Cycle 6 chaînons Cyclisation Hétérocycle azote Lactame Nitrone Propriété chimique Spectre UV Tautomérie cétoénolique Transposition chimique Alaninonitrile Pyrazin-2-one(6-amino-5-benzyl-1,2-dihydro-3-méthyl) Pyruvaldéhyde oxime
- Keyword (en)
- Model compound Equilibrium constant Six membered ring Cyclization Nitrogen heterocycle Lactam Nitrone Chemical properties Ultraviolet spectrum Keto enol tautomerism Chemical rearrangement
- Keyword (es)
- Compuesto modelo Constante equilibrio Ciclo 6 eslabones Ciclización Heterociclo nitrógeno Lactamo Nitrona Propiedad química Espectro UV Tautomería ceto-enólica Transposición 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
- 3841406
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/jo00078a038 
https://dx.doi.org/10.1021/jo00078a038
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