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A short synthesis of substituted β-hydroxy γ-butyrolactones and 2-deoxyhexofuranosides

Author
ESCUDIER, J.-M; BALTAS, M; GORRICHON, L
CNRS univ. Paul Sabatier, lab. synthèse physicochimie organique, 31062 Toulouse, France
Source

Tetrahedron letters. 1992, Vol 33, Num 11, pp 1439-1442 ; ref : 15 ref

CODEN
TELEAY
ISSN
0040-4039
Scientific domain
Biochemistry, molecular biology, biophysics; Organic chemistry
Publisher
Elsevier, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Acide Lewis Acide aldonique Aldolisation Aldéhyde Catalyse acide Cycle 3 chaînons Diastéréosélectivité Enolate Epoxyde Hydroxyester Hétérocycle oxygène Lactonisation Lithium Composé Réduction chimique Stéréosélectivité Hexonique acide(δ-O-[4-bromobenzyl]-2-désoxy)-1(4)-lactone Oxiranecarbaldéhyde(3-[(4-bromobenzyloxy) méthyl]) Oxiranepropionique acide(3-[(4-bromobenzyloxy)méthyl]-β-hydroxy) ester t-butyle
Keyword (en)
Lewis acid Aldonic acid Aldol condensation Aldehyde Acid catalysis Three membered ring Diastereoselectivity Enolate Epoxide Hydroxyester Oxygen heterocycle Lactonization Lithium Compounds Chemical reduction Stereoselectivity
Keyword (es)
Acido Lewis Acido aldónico Aldolización Aldehído Catálisis ácida Ciclo 3 eslabones Diastereoselectividad Enolato Epóxido Hidroxiester Heterociclo oxígeno Lactonización Litio Compuesto Reducción química Estereoselectividad
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
5211557

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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