About: Umberto Piarulli

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Umberto Piarulli Goto Sponge Distinct Permalink

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	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq)
rdfs:label	Umberto Piarulli (en) Umberto Piarulli (es) Umberto Piarulli (it) Umberto Piarulli (nl) Umberto Piarulli (sl) Umberto Piarulli (ast)
skos:prefLabel	Umberto Piarulli (en) Umberto Piarulli (es) Umberto Piarulli (it) Umberto Piarulli (nl) Umberto Piarulli (sl) Umberto Piarulli (ast)
name	Umberto Piarulli (en) Umberto Piarulli (es) Umberto Piarulli (it) Umberto Piarulli (nl) Umberto Piarulli (sl) Umberto Piarulli (ast)
Scopus author ID	wds:Q42741758-9D5A6198-70CB-48C6-AD28-E0C0100A78FF
Scopus author ID	6701481057
given name	wds:Q42741758-8976D738-D06F-4675-90A9-034B33BC1212
given name	Umberto
instance of	wds:Q42741758-10F7FCFC-4ED2-4BFF-9C99-2123B06D93BE
instance of	Homo sapiens
occupation	wds:Q42741758-F2B6AB0B-7DF6-4985-86F6-23DE12731FFA
employer	wds:Q42741758-9801ACAA-708D-4464-82C7-BCC568EBB9FD wds:Q42741758-A63695B6-5C4A-461E-9383-126FD76641CA
sex or gender	wds:Q42741758-2B2F30A6-CD01-4C73-A010-C8041BCCB453
VIAF ID	wds:Q42741758-30D5B866-4050-4E7A-8FBF-7CD15FF16310
IdRef ID	wds:Q42741758-9BD20DAA-028E-451F-9659-E21692606BDE
family name	wds:Q42741758-AB53EB2C-3047-49A5-BA97-B5B1A0EE481D
VIAF ID	http://viaf.org/viaf/316040851
IdRef ID	http://www.idref.fr/185757758/id
occupation	researcher
employer	University of Insubria Department of Mathematics "Federigo Enriques"
sex or gender	male
VIAF ID	316040851
IdRef ID	185757758
family name	Piarulli
ORCID iD	wds:Q42741758-80627AC9-0805-4022-B7E1-DDE3BE4E40B1
ORCID iD	https://orcid.org/0000-0002-6952-1811
ORCID iD	0000-0002-6952-1811
IRInSubria author ID	wds:Q42741758-5FA1990E-ED5C-4B5F-9D54-E11B44B01D99
IRInSubria author ID	04292
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42741758
is author of	Rhodium-catalyzed asymmetric hydrogenation of olefins with PhthalaPhos, a new class of chiral supramolecular ligands Combinatorial Libraries of Chiral Ligands for Enantioselective Catalysis Discovery of a New Efficient Chiral Ligand for Copper-Catalyzed Enantioselective Michael Additions by High-Throughput Screening of a Parallel Library Investigation of a New Family of Chiral Ligands for Enantioselective Catalysis via Parallel Synthesis and High-Throughput Screening Rh-catalyzed asymmetric hydrogenation of prochiral olefins with a dynamic library of chiral TROPOS phosphorus ligands Rh-catalyzed enantioselective conjugate addition of arylboronic acids with a dynamic library of chiral tropos phosphorus ligands A library approach to the development of BenzaPhos: highly efficient chiral supramolecular ligands for asymmetric hydrogenation Enantioselective conjugate addition of phenylboronic acid to enones catalysed by a chiral tropos/atropos rhodium complex at the coalescence temperature Supramolecular ligand-ligand and ligand-substrate interactions for highly selective transition metal catalysis. PhthalaPhos: Chiral Supramolecular Ligands for Enantioselective Rhodium-Catalyzed Hydrogenation Reactions Chiral (salen)Co(III)(N-benzyl-l-serine)-derived phosphites: monodentate P-ligands for enantioselective catalytic applications Combinations of Acidic and Basic Monodentate Binaphtholic Phosphites as Supramolecular Bidentate Ligands for Enantioselective Rh-Catalyzed Hydrogenations Combination of a binaphthol-derived phosphite and a C1-symmetric phosphinamine generates heteroleptic catalysts in Rh- and Pd-mediated reactions Highly enantioselective Rh-catalyzed hydrogenations with heterocombinations of pentafluorobenzyl- and methoxybenzyl-derived binaphthyl phosphites Synthesis and biological evaluation (in vitro and in vivo) of cyclic arginine-glycine-aspartate (RGD) peptidomimetic-paclitaxel conjugates targeting integrin αVβ3. Computational design of novel peptidomimetic inhibitors of cadherin homophilic interactions Cyclic isoDGR and RGD peptidomimetics containing bifunctional diketopiperazine scaffolds are integrin antagonists. Combinatorial Libraries: Studies in Molecular Recognition and the Quest for New Catalysts Effect of Ligands and Additives on the Palladium-Promoted Carbonylative Coupling of Vinyl Stannanes and Electron-Poor Enol Triflates Determination of the binding epitope of RGD-peptidomimetics to αvβ3 and α(IIb)β3 integrin-rich intact cells by NMR and computational studies. Cyclic RGD Peptidomimetics Containing Bifunctional Diketopiperazine Scaffolds as New Potent Integrin Ligands Effects of a novel cyclic RGD peptidomimetic on cell proliferation, migration and angiogenic activity in human endothelial cells Synthesis of (S)- and (R)-5-oxo-piperazine-2-carboxylic acid and its application to peptidomimetics Toward the first nonpeptidic molecular tong inhibitor of wild-type and mutated HIV-1 protease dimerization Discovery of a new efficient chiral ligand for copper-catalyzed enantioselective Michael additions by high-throughput screening of a parallel library. Copper Phosphoramidite-Catalyzed Enantioselective Desymmetrization ofmeso-Cyclic Allylic Bisdiethyl Phosphates Metallohosts Derived from the Assembly of Sugars around Transition Metals: The Complexation of Alkali Metal Cations Synthesis, Characterization, and Biological Evaluation of a Dual-Action Ligand Targeting αvβ3 Integrin and VEGF Receptors Synthesis and biological evaluation of RGD peptidomimetic-paclitaxel conjugates bearing lysosomally cleavable linkers Tumor Targeting with an isoDGR-Drug Conjugate Cyclic RGD-peptidomimetics containing bifunctional diketopiperazine scaffolds as new potent integrin ligands. Cyclic isoDGR peptidomimetics as low-nanomolar αvβ3 integrin ligands. Synthesis of [Bis(hexamethylene)cyclopentadienone]iron Tricarbonyl and its Application to the Catalytic Reduction of C=O Bonds Expanding the Catalytic Scope of (Cyclopentadienone)iron Complexes to the Hydrogenation of Activated Esters to Alcohols Synthesis of (R)-BINOL-Derived (Cyclopentadienone)iron Complexes and Their Application in the Catalytic Asymmetric Hydrogenation of Ketones Chiral (Cyclopentadienone)iron Complexes for the Catalytic Asymmetric Hydrogenation of Ketones Bifunctional 2,5-Diketopiperazines as Rigid Three-Dimensional Scaffolds in Receptors and Peptidomimetics Insights into the Binding of Cyclic RGD Peptidomimetics to α5β1 Integrin by using Live-Cell NMR And Computational Studies A new method for the solution and solid phase synthesis of chiral β-sulfonopeptides under mild conditions

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 194 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software