Synthesis of C-4 substituted pyrimidine nucleoside analogs. Preparation of several 4-(2-oxoalkylidene)-2(1H)-pyrimidinone ribonucleosides
- Author
- ACEVEDO, O. L; ANDREWS, R. S; DUNKEL, M; COOK, P. D
ISIS Pharmaceuticals, Inc., medicinal chemistry dep., Carlsbad CA 92008, United States - Source
Journal of heterocyclic chemistry. 1994, Vol 31, Num 4, pp 989-995
- CODEN
- JHTCAD
- ISSN
- 0022-152X
- Scientific domain
- Organic chemistry
- Publisher
- HeteroCorporation, Odessa, FL
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Appariement base Complexe chloro Composé acétylénique Copulation chimique Enamine Enol Guanosine Liaison hydrogène Palladium II Complexe Pyrimidine nucléoside Ribonucléoside Réaction catalytique Hex-2-yne Pyrimidin-2-one(1,2-dihydro-4-[2-hydroxyhex-1-ényl]-1-β-D-ribofuranosyl) Pyrimidin-2-one(1,2-dihydro-4-hex-1-ynyl-1-[tri-O-benzoyl-β-D-ribofuranosyl]) Pyrimidin-2-one(4-[2-aminohex-1-ényl]-1,2-dihydro-1-β-D-ribofuranosyl) Pyrimidin-2-one(4-chloro-1,2-dihydro-1-[tri-O-benzoyl-β-D-ribofuranosyl]) Triphénylphosphine Métal divalent Complexe
- Keyword (en)
- Base pairing Chloro complex Acetylenic compound Chemical coupling Enamine Enol Guanosine Hydrogen bond Palladium II Complexes Pyrimidine nucleoside Ribonucleoside Catalytic reaction Divalent metal Complexes
- Keyword (es)
- Apareamiento base Complejo cloro Compuesto acetilénico Copulación química Enamina Enol Guanosina Enlace hidrógeno Paladio II Complejo Pirimidina nucleósido Ribonucleósido Reacción catalítica Metal divalente Complejo
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C07 Carbohydrates. Nucleosides and nucleotides / 001C03C07B Nucleosides, nucleotides and oligonucleotides
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4245563
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.5570310449 
https://dx.doi.org/10.1002/jhet.5570310449
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