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4-O-Benzyl-2,3-O-isopropylidene-D-erythrose and -D-threose from 2,3-O-isopropylidene-D-glyceraldehyde via thiazole intermediates. Synthesis of 2-deoxykanosamine

Author
DONDONI, A; MERINO, P
Univ., dip. chimica, lab. chimia organia, Ferrara, Italy
Source

Synthesis (Stuttgart). 1992, Num 1-2, pp 196-200 ; ref : 14 ref

CODEN
SYNTBF
ISSN
0039-7881
Scientific domain
Organic chemistry
Publisher
Thieme, New York, NY / Thieme, Stuttgart
Publication country
Germany
Document type
Article
Language
English
Keyword (fr)
Addition Michaël Aldose Allongement chaîne Aminoglycoside Cycle 5 chaînons Hétérocycle soufre azote Réaction Wittig Silane organique Silicium Composé organique Arabinopyranoside(6-O-benzyl-3-benzylamino-2,3-didésoxy-1-O-méthyl) Erythrose(4-O-benzyl-2,3-O-isopropylidène) Glycéraldéhyde(2,3-O-isopropylidène) Thiazole(2-triméthylsilyl) Thréose(4-O-benzyl-2,3-O-isopropylidène)
Keyword (en)
Michael addition Aldose Chain elongation Aminoglycoside Five membered ring Sulfur nitrogen heterocycle Wittig reaction Organic silane Silicon Organic compounds
Keyword (es)
Adición Michael Aldosa Alargamiento cadena Aminoglicósido Ciclo 5 eslabones Heterociclo azufre nitrógeno Reacción Wittig Silano orgánico Silicio Compuesto orgánico
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
5120036

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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