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Glucosylation of some steroidal 17-hydroxy derivatives

Author
CERNY, I; POUZAR, V; DRASAR, P; HAVEL, M
Czechoslovak acad. sci., inst. organic chemistry biochemistry, Prague 166 10, Czechoslovakia
Source

Collection of Czechoslovak chemical communications. 1992, Vol 57, Num 2, pp 362-374 ; ref : 12 ref

CODEN
CCCCAK
ISSN
0010-0765
Scientific domain
Chemistry
Publisher
Czechoslovak Academy of Sciences, Institute of Organic Chemistry and Biochemistry, Praha
Publication country
Czech Republic
Document type
Article
Language
English
Keyword (fr)
Acylate Alcool secondaire Argent I Silicate Composé aromatique Composé saturé Composé éthylénique Glycoside Glycosylation Glycosyle halogénure Réaction catalytique Stéroïde Androst-5-ene-3,3,17diol 3β-acétate Androst-5-én-3β-ol (17-β-D-glucopyranosyloxy) Androstane-3β,17β-diol 3β-nitrate Gestra-1,3,5(10)-trién-3-ol (17-β-D-glucopyranosyloxy) Glucopyranosyle (tétra-O-acétyl) bromure gestradiol 3-acétate
Keyword (en)
Acylate Secondary alcohol Silver I Silicates Aromatic compound Saturated compound Ethylenic compound Glycoside Glycosylation Glycosyl halogenide Catalytic reaction Steroid
Keyword (es)
Acilato Alcohol secundario Plata I Silicato Compuesto aromático Compuesto saturado Compuesto etilénico Glicósido Glicosilación Glicosilo halogenuro Reacción catalítica Esteroide
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
5217375

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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