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A two-step efficient chemoenzymatic synthesis of flavonoid glycoside malonates

Author
RIVA, S1 ; DANIELI, B; LUISETTI, M
[1] CNR, Istituto di Chimica degli Ormoni, via Mario Bianco 9, 20131 Milano, Italy
Source

Journal of natural products (Print). 1996, Vol 59, Num 6, pp 618-621

CODEN
JNPRDF
ISSN
0163-3864
Scientific domain
Pharmacology drugs
Publisher
American Chemical Society, Washington, DC / American Society of Pharmacognosy, Glendale, AZ
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Acylation Aldose Diholoside Débenzylation Flavonoïde Glycoside Réaction enzymatique Régiosélectivité Triacylglycerol lipase Flavanone dérivé Flavone dérivé Isoquercitrine(6p-O-hydroxymalonyl) Malonique acide ester dibenzyle Naringine(6p-O-hydroxymalonyl) Rutine(3p-O-hydroxymalonyl) Carboxylic ester hydrolases Enzyme Esterases Hydrolases
Keyword (en)
Acylation Aldose Disaccharide Debenzylation Flavonoid Glycoside Enzymatic reaction Regioselectivity Triacylglycerol lipase Carboxylic ester hydrolases Enzyme Esterases Hydrolases
Keyword (es)
Acilación Aldosa Diholosido Debencilación Flavonoide Glicósido Reacción enzimática Regioselectividad Triacylglycerol lipase Carboxylic ester hydrolases Enzima Esterases Hydrolases
Classification
Pascal
002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A31 Biotechnology / 002A31C Methods. Procedures. Technologies / 002A31C06 Bioconversions. Hemisynthesis

Discipline
Biotechnology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
3123937

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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