About: Renzo Luisi

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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	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) wetenschapper (nl) дослідник (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq)
rdfs:label	Renzo Luisi (en) Renzo Luisi (es) Renzo Luisi (it) Renzo Luisi (nl) Renzo Luisi (sl) Renzo Luisi (ast)
skos:prefLabel	Renzo Luisi (en) Renzo Luisi (es) Renzo Luisi (it) Renzo Luisi (nl) Renzo Luisi (sl) Renzo Luisi (ast)
name	Renzo Luisi (en) Renzo Luisi (es) Renzo Luisi (it) Renzo Luisi (nl) Renzo Luisi (sl) Renzo Luisi (ast)
IRIS UNIBA author ID	wds:Q41531272-CCEAB0C0-7B30-4CAA-8C24-6F698C8B4CD0
IRIS UNIBA author ID	06750
Scopus author ID	wds:Q41531272-02EBA672-B55D-4E6D-83BA-F26F0C02416C
Scopus author ID	6603678250
given name	wds:Q41531272-5204B433-80B2-48DF-9EF7-DB6B544BAFC9
given name	Renzo
instance of	wds:Q41531272-1D4EA7D5-C573-488E-AAB6-E4F8C486FB05
instance of	Homo sapiens
Loop ID	wds:Q41531272-1BFC815A-6084-4284-BE95-A0C4753E685F
Loop ID	745328
occupation	wds:Q41531272-5C644EB6-21C6-4E76-BBBC-BAABC8F0F3B8
NUKAT ID	wds:Q41531272-26E8FCC7-93CC-4DA8-A462-556E1F0FF842
sex or gender	wds:Q41531272-1CB4A6C2-E6AC-4935-8371-2F431F8A7998
ISNI	wds:Q41531272-ABD474A4-458A-4476-A047-B9FCF58C6D1E
VIAF ID	wds:Q41531272-CA0BFF57-F24E-4B56-B223-08A4EF73EEE8
GND ID	wds:Q41531272-a363e2c2-c1c5-499d-8b19-5193cccabbdc
IdRef ID	wds:Q41531272-135EC713-087F-4953-A12C-9BDF6E9D8A18
date of birth	wds:Q41531272-D9298BE8-FD37-4F47-861E-2C87A1CDD5B8
family name	wds:Q41531272-CDA3780E-A6BE-4CF0-A9D2-E201A0CAC8A9
WorldCat Identities ID (superseded)	wds:Q41531272-003B3181-A968-4FC1-94D4-42D9C080E3BA
VIAF ID	http://viaf.org/viaf/308190566
GND ID	https://d-nb.info/gnd/1051321441
IdRef ID	http://www.idref.fr/181847256/id
occupation	researcher
NUKAT ID	n2014094455
sex or gender	male
ISNI	0000000433657156
VIAF ID	308190566
GND ID	1051321441
IdRef ID	181847256
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
family name	Luisi
WorldCat Identities ID (superseded)	viaf-310507910
ORCID iD	wds:Q41531272-AFC79333-9301-4694-B25B-33C225350386
ORCID iD	https://orcid.org/0000-0002-9882-7908
ORCID iD	0000-0002-9882-7908
ResearcherID	wds:Q41531272-1ED02554-706A-458A-9D1A-A428F3A5D784
Publons author ID	wds:Q41531272-b4c19e94-59eb-4b16-b5b9-f019db304a04
ResearcherID	F-5636-2016
Publons author ID	1307672
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q41531272
is author of	Recent advances in the stereoselective synthesis of aziridines. Oxiranyl anion-mediated synthesis of highly enantiomerically enriched styrene oxide derivatives New anti-viral drugs for the treatment of the common cold Aziridinyl anions: generation, reactivity, and use in modern synthetic chemistry. Michael addition of chloroalkyloxazolines to electron-poor alkenes: synthesis of heterosubstituted cyclopropanes. Metalation of 2-chloromethyl-2-oxazolines: synthesis of 1,2,3-tris(oxazolinyl)cyclopropanes and derivatives Asymmetric synthesis of cyclopropanes from lithiated aryloxiranes and alpha,beta-unsaturated Fischer carbene complexes Transfer of Electrophilic NH Using Convenient Sources of Ammonia: Direct Synthesis of NH Sulfoximines from Sulfoxides Pharmaceutical development of novel lactate-based 6-fluoro-l-DOPA formulations. Harnessing the ortho-directing ability of the azetidine ring for the regioselective and exhaustive functionalization of arenes. Alpha-substituted alpha-lithiated oxiranes: useful reactive intermediates. Stereospecific synthesis of optically active phenylpropylene oxides Regio- and stereoselective lithiation and electrophilic substitution reactions of N-Alkyl-2,3-diphenylaziridines: solvent effect. Synthetic approach to substituted cyclopropanes based on the coupling reaction of lithiated chloroalkyloxazolines with Fischer carbene complexes Exploiting a "Beast" in Carbenoid Chemistry: Development of a Straightforward Direct Nucleophilic Fluoromethylation Strategy A direct and sustainable synthesis of tertiary butyl esters enabled by flow microreactors. Alpha- vs ortho-lithiation of N-alkylarylaziridines: probing the role of the nitrogen inversion process Directed ortho lithiation of N-alkylphenylaziridines Synthesis of NH-sulfoximines from sulfides by chemoselective one-pot N- and O-transfers. Carbolithiation of S-alkenyl-N-aryl thiocarbamates: carbanion arylation in a connective route to tertiary thiols. A greener and efficient access to substituted four- and six-membered sulfur-bearing heterocycles. Synthesis of optically active arylaziridines by regio- and stereospecific lithiation of N-bus-phenylaziridine Recent advances in the chemistry of metallated azetidines. Azetidine-Borane Complexes: Synthesis, Reactivity, and Stereoselective Functionalization Stereocontrolled lithiation/trapping of chiral 2-alkylideneaziridines: investigation into the role of the aziridine nitrogen stereodynamics One-pot preparation of piperazines by regioselective ring-opening of non-activated arylaziridines

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