Stereoselective synthesis of a C-glycoside analogue of N-Fmoc-serine β-N-acetylglucosaminide by Ramberg-Bäcklund rearrangement
- Author
- OHNISHI, Yuki1 ; ICHIKAWA, Yoshitaka1
[1] Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21205, United States - Source
Bioorganic & medicinal chemistry letters (Print). 2002, Vol 12, Num 7, pp 997-999
- ISSN
- 0960-894X
- Scientific domain
- Biochemistry, molecular biology, biophysics; Pharmacology drugs
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aminoglycoside C-Glycoside Stéréosélectivité Synthèse chimique α-Aminoacide Butyrique acide(4-[2-acétamido-2-désoxy-3,4,6-tri-O-acétyl-β-D-glucopyranosyl]-2-[fluorén-9-ylméthoxycarbonylamino]) Réaction Ramberg Bäcklung
- Keyword (en)
- Aminoglycoside C-Glycoside Stereoselectivity Chemical synthesis α-Aminoacid Ramberg Bäcklung reaction
- Keyword (es)
- Aminoglicósido C-Glicósido Estereoselectividad Síntesis química α-Aminoácido
- 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
- 13541371
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
10.1016/S0960-894X(02)00104-X 
https://dx.doi.org/10.1016/S0960-894X(02)00104-X
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