About: Pietro Allevi

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	researcher (en) 연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy)
rdfs:label	Pietro Allevi (en) Pietro Allevi (es) Pietro Allevi (it) Pietro Allevi (nl) Pietro Allevi (ast)
skos:prefLabel	Pietro Allevi (en) Pietro Allevi (es) Pietro Allevi (it) Pietro Allevi (nl) Pietro Allevi (ast)
name	Pietro Allevi (en) Pietro Allevi (es) Pietro Allevi (it) Pietro Allevi (nl) Pietro Allevi (ast)
Scopus author ID	wds:Q56527558-AF4E40D4-9D4C-47CF-977A-5C5E7CD0C7F1
Scopus author ID	7004617754
given name	wds:Q56527558-34A97EF2-8ECC-4D5E-9D8F-D7BA22094BF9
given name	Pietro
instance of	wds:Q56527558-C92528C0-B83E-4CF2-8191-104FCDAF5E49
instance of	Homo sapiens
occupation	wds:Q56527558-0F0ACAEB-908B-478C-B7BD-CEBB39C115B3
employer	wds:Q56527558-2AA4F364-E1E7-4E27-B5C9-A099D20E296D wds:Q56527558-57C993E4-ABAD-4893-928D-6860D3C58EDB wds:Q56527558-CF32D21F-B3FF-4924-A324-811266AF7B37
sex or gender	wds:Q56527558-BB41D50C-013F-42F2-84A6-842E2A509451
VIAF ID	wds:Q56527558-A68FE3F8-D69E-4034-89A1-EE9E009EB5FD
SBN author ID	wds:Q56527558-3CA4984F-AE86-4ED8-8FBF-5E12B6F697AC
SHARE Catalogue author ID	wds:Q56527558-E89CEB63-2129-404E-8B61-9B98C2A77F12
family name	wds:Q56527558-B1A7279E-CBC8-4699-A2A1-06540929173A
VIAF ID	http://viaf.org/viaf/90375207
occupation	researcher
employer	University of Milan Department of Mathematics "Federigo Enriques"
sex or gender	male
VIAF ID	90375207
SBN author ID	TSAV008499
SHARE Catalogue author ID	66588
family name	Allevi
ORCID iD	wds:Q56527558-5FEC165B-50AB-4141-A332-A810A63A9348
ORCID iD	https://orcid.org/0000-0002-9525-0154
ORCID iD	0000-0002-9525-0154
IRIS UNIMI author ID	wds:Q56527558-EE662DBB-B699-4760-BF74-BA935C5BE657
IRIS UNIMI author ID	02522
ResearcherID	wds:Q56527558-6C10FEAE-A174-4C69-9CF1-DD0671A7D0C5
ResearcherID	P-6666-2017
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56527558
is author of	Practical syntheses of pyridinolines, important amino acidic biomarkers of collagen health A simple synthesis of N-perfluoroacylated and N-acylated glycals of neuraminic acid with a cyclic aminic substituent at the 4α position as possible inhibitors of sialidases. Beta-ethoxyacrolein contamination increases malondialdehyde inhibition of milk xanthine oxidase activity Free and total malondialdehyde assessment in biological matrices by gas chromatography-mass spectrometry: what is needed for an accurate detection Chemoselective synthesis of sialic acid 1,7-lactones. Reaction of N-acetylneuraminic acid derivatives with perfluorinated anhydrides: a short access to N-perfluoracylated glycals with antiviral properties. Synthesis and biological evaluation of several dephosphonated analogues of CMP-Neu5Ac as inhibitors of GM3-synthase. The first total synthesis of carminic acid Evidence for the presence of 7-hydroperoxycholest-5-en-3 beta-ol in oxidized human LDL. Stereochemical course of the hydroboration of highly hindered steroidal olefins. A ready synthesis of 14 beta- and 8 alpha,14 beta-steroids Structural requirements of aldehydes produced in LPO for the activation of the heat-shock genes in HeLa cells Inhibition of in vitro lipid peroxidation by stable steroidic nitroxyl radicals Synthesis and aggregative properties of GM1 ganglioside (IV3Neu5AcGgOse4Cer) containing D-(+)-2-hydroxystearic acid. Synthesis of 14 beta-cholesta-5,7-dien-3 beta-ol The first synthesis of glucosylgalactosyl hydroxylysine (Glu-Gal-Hyl), an important biological indicator of collagen turnover. The first total synthesis of alpha-D-glucopyranosyl-(1-->2)-beta-D-galactopyranosyl-O-pyridinoline, an important hallmark of human joint diseases. General and chemoselective N-transacylation of secondary amides by means of perfluorinated anhydrides Elucidation of several neglected reactions in the GC-MS identification of sialic acids as heptafluorobutyrates calls for an urgent reassessment of previous claims Synthesis and chemical characterization of several perfluorinated sialic acid glycals and evaluation of their in vitro antiviral activity against Newcastle disease virus pH sensitivity and plasma stability of liposomes containing N-stearoylcysteamine C-Glucopyranosyl derivatives from readily available 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl chloride Simultaneous free and glycosylated pyridinium crosslink determination in urine: validation of an HPLC-fluorescence method using a deoxypyridinoline homologue as internal standard A new convenient transformation of erythromycin A into clarithromycin Correction: The first synthesis of N-acetylneuraminic acid 1,7-lactone Mechanisms of action of malondialdehyde and 4-hydroxynonenal on xanthine oxidoreductase. A convenient isomerization of 6-oxo-3 alpha,5-cyclo-5 alpha-steroids to 6-oxo-delta 2-5 alpha-steroids Sterol synthesis : chemical synthesis of 3 beta-hydroxy-5 alpha-cholest-7-ene-9 alpha-carbonitrile Synthesis of 7 alpha,12 alpha-dihydroxy-3 alpha- [2-(beta-D-glucopyranosyl)acetyl]-5 beta-cholan-24-oic acid Evaluation of the oral toxicity of spinacine hydrochloride in a 13-week study in rats Elucidation of the opening of the epoxidic ring of the 3beta-acetoxy-14alpha,15alpha-epoxy-5alpha-cholest-8-en-7-one by methanol, using NMR techniques assisted by a conformational study through theoretical calculations Correction to "chemoselective synthesis of sialic Acid 1,7-lactones" Revised Structures for the Lactones Obtained by Reduction of the Adduct of Ergosterol Acetate with Maleic Anhydride Synthesis of (E)-9-(1-pyrenyl)-4-hydroxynon-2-enal, a fluorescent probe of the (E)-4-hydroxynon-2-enal with retained biological properties
is author of	wds:Q51710814-494FEFA0-377E-47D2-A17F-85376F90D535 wds:Q56268327-BCD75EB9-3EA8-42D0-A099-562BD5B925F9 wds:Q68976973-3659D93D-A4E9-4347-9576-E9ED975DE6AE wds:Q73740807-EAFDA851-56D9-478A-A3BA-7A9C56311891 wds:Q80068764-4259B8FC-DCD9-4B3A-B0AB-CE35AC69F3B3 wds:Q57076182-E5F87E6D-AF66-4934-98DD-8974879BDD98 wds:Q68713353-28197B3A-15CE-4872-914B-010199D009EB wds:Q84797575-174BA261-58B9-458C-BE9E-E80A4ADD4CC3 wds:Q77583718-4E377C51-3318-490F-8BA5-073ED5D7C4FA

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