http://www.cnr.it/ontology/cnr/individuo/prodotto/ID188114
Biotransformation of spirolaxine by Absidia cuneospora and Trametes hirsuta: Formation of beta-glycosyl and beta-xylosyl derivatives (Articolo in rivista)
- Type
- Label
- Biotransformation of spirolaxine by Absidia cuneospora and Trametes hirsuta: Formation of beta-glycosyl and beta-xylosyl derivatives (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.molcatb.2012.06.006 (literal)
- Alternative label
Bava, Adriana; Nasini, Gianluca; Fronza, Giovanni (2012)
Biotransformation of spirolaxine by Absidia cuneospora and Trametes hirsuta: Formation of beta-glycosyl and beta-xylosyl derivatives
in Journal of molecular catalysis. B, Enzymatic (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Bava, Adriana; Nasini, Gianluca; Fronza, Giovanni (literal)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
- Note
- ISI Web of Science (WoS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Polytechnic University of Milan (literal)
- Titolo
- Biotransformation of spirolaxine by Absidia cuneospora and Trametes hirsuta: Formation of beta-glycosyl and beta-xylosyl derivatives (literal)
- Abstract
- Incubation of spirolaxine 1a with the fungus Absidia cuneospora afforded 5 beta-glucosyl-spirolaxine 2b; the structure of the biotransformed product was deduced on the basis of MS. NMR data and chemical semi-synthesis. When using Trametes hirsuta as a bioagent 1a afforded 5 beta-xylosyl-spirolaxine 3a; the identification of the sugar moiety came from acidic hydrolysis of the new metabolite. (c) 2012 Elsevier B.V. All rights reserved. (literal)
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