A totally synthetic route to enantiomerically pure D and L-aminooctoses : stereocontrolled synthesis of methyl α-D-lincosaminide
- Author
- SZECHNER, B; ACHMATOWICZ, O
Warsaw agricultural univ., inst. gen. chemistry, Warsaw, Poland - Source
Journal of carbohydrate chemistry. 1992, Vol 11, Num 3, pp 401-406 ; ref : 14 ref
- CODEN
- JCACDM
- ISSN
- 0732-8303
- Scientific domain
- Organic chemistry
- Publisher
- Dekker, Monticello, NY
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aldéhyde Aminoglycoside Cycle 5 chaînons Hétérocycle oxygène azote Hétérocycle oxygène Stéréosélectivité Synthèse totale Furane(perhydro) Lincosaminide Oxazolidine-4-carbaldéhyde(3-benzènesulfonyl-2,2,5-triméthyl)
- Keyword (en)
- Aldehyde Aminoglycoside Five membered ring Oxygen nitrogen heterocycle Oxygen heterocycle Stereoselectivity Total synthesis
- Keyword (es)
- Aldehído Aminoglicósido Ciclo 5 eslabones Heterociclo oxígeno nitrógeno Heterociclo oxígeno Estereoselectividad Síntesis total
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C07 Carbohydrates. Nucleosides and nucleotides / 001C03C07A Carbohydrates with 4, 5, 6, ... C atoms, dissacharides and oligosaccharides
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5272581
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
10.1080/07328309208018002 
https://dx.doi.org/10.1080/07328309208018002
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