About: Armido Studer

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

organic chemist

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) 연구원 (ko) 研究者 (ja) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) organic chemist (en) švýcarský profesor organické chemie (cs)
rdfs:label	Armido Studer (cs) Armido Studer (en) Armido Studer (es) Armido Studer (nl) Armido Studer (sk) Armido Studer (sq) Armido Studer (ast)
skos:prefLabel	Armido Studer (cs) Armido Studer (en) Armido Studer (es) Armido Studer (nl) Armido Studer (sk) Armido Studer (sq) Armido Studer (ast)
name	Armido Studer (cs) Armido Studer (en) Armido Studer (es) Armido Studer (nl) Armido Studer (sk) Armido Studer (sq) Armido Studer (ast)
instance of	wds:Q56954265-3908C92E-AD08-4DE9-BF4D-46B253387B54
NL CR AUT ID	wds:Q56954265-C3DAA093-A666-4DA5-AE13-AA025B1C2599
instance of	Homo sapiens
NL CR AUT ID	mub2014840505
Academic Tree ID	wds:Q56954265-4735F1E9-D2D6-412B-9AEE-78B22E6C746D
Academic Tree ID	99040
occupation	wds:Q56954265-2AC92DAE-A885-4AC9-89D3-EF8E7093B83A
NUKAT ID	wds:Q56954265-DBC186A5-5102-4956-AEA2-6E7CC8BD4B82
sex or gender	wds:Q56954265-9b72d851-14a5-4e5d-9223-5d2cd1f00254
ISNI	wds:Q56954265-D75B4181-A706-493B-B913-84BCD9EDBDA0
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GND ID	wds:Q56954265-d15143e6-0e9e-4656-9562-f5fcb2c97c1f
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date of birth	wds:Q56954265-87BD9519-D7BA-4DEE-8FBF-E88FADFEED57
family name	wds:Q56954265-430F70BB-1F64-4280-AF28-36D909FC549E
National Library of Israel J9U ID	wds:Q56954265-42B5D8AA-4ADC-42E2-9F08-44811CAB67FE
VIAF ID	http://viaf.org/viaf/187017244
GND ID	https://d-nb.info/gnd/1261076915
IdRef ID	http://www.idref.fr/160378710/id
occupation	researcher
NUKAT ID	n2012212013
sex or gender	male
ISNI	0000000356628991
VIAF ID	187017244
GND ID	1261076915
IdRef ID	160378710
date of birth	1967-01-01 00:00:00Z (xsd:dateTime)
family name	Studer
National Library of Israel J9U ID	987007423563905171
ORCID iD	wds:Q56954265-4F083579-D0A9-47CA-9B69-B3C05AB560D6
ORCID iD	https://orcid.org/0000-0002-1706-513X
ORCID iD	0000-0002-1706-513X
SNSF person ID	wds:Q56954265-012BAD2E-5572-43E7-948D-E718AE8691D9
SNSF person ID	57893
is owl:sameAs of	Armido Studer
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56954265
is author of	Nitroxides: applications in synthesis and in polymer chemistry Structural requirements for optimized delivery, inhibition of oxidative stress, and antiapoptotic activity of targeted nitroxides Transition-Metal-Free Oxidative Homocoupling of Aryl, Alkenyl, and Alkynyl Grignard Reagents with TEMPO A "Renaissance" in radical trifluoromethylation Catalysis of Radical Reactions: A Radical Chemistry Perspective The electron is a catalyst Enantioselective cyclopropanation of enals by oxidative N-heterocyclic carbene catalysis. Nitroxide-Mediated Polymerization ofN-Isopropylacrylamide: Electrospray Ionization Mass Spectrometry, Matrix-Assisted Laser Desorption Ionization Mass Spectrometry, and Multiple-Angle Laser Light Scattering Studies on Nitroxide-Terminated Poly-N-isop Sulfonium Ylides by (3+2) Cycloaddition of Arynes with Vinyl Sulfides: Stereoselective Synthesis of Highly Substituted Alkenes. Catalysis with N-heterocyclic carbenes under oxidative conditions Biomimetic carbene-catalyzed oxidations of aldehydes using TEMPO. Oxidative homocoupling of aryl, alkenyl, and alkynyl Grignard reagents with TEMPO and dioxygen Cooperative Magnetism in Crystalline N-Aryl-Substituted Verdazyl Radicals: First-Principles Predictions and Experimental Results Black-box determination of temperature-dependent susceptibilities for crystalline organic radicals with complex magnetic topologies Effect of the C(3)-Substituent in Verdazyl Radicals on their Profluorescent Behavior. Synthesis of Chiral Piperazinones Using Amphoteric Aziridine Aldehyde Dimers and Functionalized Isocyanides Intra- versus intermolecular electron transfer in radical nucleophilic aromatic substitution of dihalo(hetero)arenes - a tool for estimating π-conjugation in aromatic systems Silylated cyclohexadienes as new radical chain reducing reagents: preparative and mechanistic aspects Oxidative biaryl coupling of thiophenes and thiazoles with arylboronic acids through palladium catalysis: otherwise difficult C4-selective C-H arylation enabled by boronic acids. Short and Divergent Total Synthesis of (+)-Machaeriol B, (+)-Machaeriol D, (+)-Δ(8)-THC, and Analogues. N,N-addition of frustrated Lewis pairs to nitric oxide: an easy entry to a unique family of aminoxyl radicals. Synthesis and characterization of inorganic-organic hybrid materials based on the intercalation of stable organic radicals into a fluoromica clay Intramolecular radical hydrosilylation--the first radical 5-endo-dig cyclisation Memory of axial chirality in aryl radical phosphanylations. Patterning of functional compounds by multicomponent Langmuir-Blodgett transfer and subsequent chemical modification Stereoselective palladium-catalyzed carboaminoxylations of indoles with arylboronic acids and TEMPO. Hydroxy- and silyloxy-substituted TEMPO derivatives for the living free-radical polymerization of styrene and n-butyl acrylate: synthesis, kinetics, and mechanistic studies Stereospecific formal [3+2] dipolar cycloaddition of cyclopropanes with nitrosoarenes: an approach to isoxazolidines. Tin-free radical chemistry using the persistent radical effect: alkoxyamine isomerization, addition reactions and polymerizations Chemical modification of polymer brushes via nitroxide photoclick trapping

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