Oxetanocin-oxetanose chemistry : lewis acid promoted glycosidations of the D-erythrooxetanose derivatives
- Author
- NISHIYAMA, S; OHGIYA, T; YAMAMURA, S; KATO, K; TAKITA, T
Keio univ., fac. sci., dep. chemistry, Hiyoshi, Yokohama 223, Japan - Source
Nucleosides & nucleotides. 1992, Vol 11, Num 2-4, pp 417-436 ; ref : 13 ref
- CODEN
- NUNUD5
- ISSN
- 0732-8311
- Scientific domain
- Biotechnology; Organic chemistry
- Publisher
- Dekker, Monticello, NY
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acide Lewis Alditol Aldose Catalyse acide Cycle 4 chaînons Cycle 5 chaînons Hétérocycle oxygène Purine nucléoside Silicium Composé organique Adénine(n6-benzoyl-9-[2,3-di-O-acyl-β-D-érythrofuranosyl]) Erythrooxétanose(1-O-acétyl) Hept-1-énitol(7-O-méthyl-4,5,6-tri-O-benzyl-1,2,3-tridésoxy) Silane(allyl triméthyl)
- Keyword (en)
- Lewis acid Alditol Aldose Acid catalysis Four membered ring Five membered ring Oxygen heterocycle Purine nucleoside Silicon Organic compounds
- Keyword (es)
- Acido Lewis Alditol Aldosa Catálisis ácida Ciclo 4 eslabones Ciclo 5 eslabones Heterociclo oxígeno Purina nucleósido Silicio Compuesto orgánico
- 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
- 5358458
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
10.1080/07328319208021715 
https://dx.doi.org/10.1080/07328319208021715
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