F
Francesca Pelizzoni
Researcher at University of Milan
Publications - 57
Citations - 1142
Francesca Pelizzoni is an academic researcher from University of Milan. The author has contributed to research in topics: Pseudomonas fluorescens & Nucleophilic addition. The author has an hindex of 19, co-authored 57 publications receiving 1102 citations.
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Bioconversion of substituted naphthalenes to the corresponding salicylic acids
Giuseppina Bestetti,P. Di Gennaro,Enrica Galli,B. Leoni,Francesca Pelizzoni,Guido Sello,Daniele Bianchi +6 more
TL;DR: The Pseudomonas fluorescens N3 strain was isolated from soil for its ability to utilize naphthalene as a carbon source as discussed by the authors, and the strain transforms 2,3-dimethyl-, 2-methoxy-, 1-and 2-ethylnaphthalenes to the corresponding salicylic acids competitively with chemical synthesis.
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Terpenoids from copaifera langsdorfii
TL;DR: The oleoresin of Copaifera langsdorfii L has been found to contain some sesquiterpenic hydrocarbons and diterpenics.
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Cycloartane triterpene glycosides from EgyptianAstragalus species
Nadia A. El-Sebakhy,Fathalla M. Harraz,Rokia M. Abdallah,Aya M. Asaad,Fulvia Orsini,Francesca Pelizzoni,Guido Sello,Luisella Verotta +7 more
TL;DR: Tomentoside I, a new tetranor-cycloartane triterpene glycoside was isolated from Astragalus tomentosus and its structure was established as 6α-acetoxy-23-ethoxy-16β,23(R)-epoxy-24,25,26,27-tetranor, 9,19-cyclolanosta-3β-O-xyloside, on the basis of spectral evidence.
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A cobalt-phosphine complex as mediator in the formation of carbon-carbon bonds
TL;DR: In this article, the complex [Co(P(CH{sub 3} ),sub 3 },sub 4] was found to mediate the Reformatsky-type reaction of halogenated esters, lactones, or amides with carbonyl compounds (ketones, aldehydes).
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Regioselective hydroxylation of chlorobenzene and chlorophenols by a Pseudomonas putida
TL;DR: Pseudomonas putida MST was able to modify halogenated aromatic compounds by co-oxidation and regiospecifically hydroxylates chlorobenzene and 2-chlorophenol to 3-chlorocatechol, and 4- chlorophenols to 4-chlorocatedchol.