About: Armando Carlone

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

researcher ORCID ID = 0000-0003-2983-6445

Attributes	Values
rdf:type	Item
description	forskare (sv) 연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) researcher ORCID ID = 0000-0003-2983-6445 (en)
rdfs:label	Armando Carlone (en) Armando Carlone (es) Armando Carlone (it) Armando Carlone (nl) Armando Carlone (ast)
skos:prefLabel	Armando Carlone (en) Armando Carlone (es) Armando Carlone (it) Armando Carlone (nl) Armando Carlone (ast)
name	Armando Carlone (en) Armando Carlone (es) Armando Carlone (it) Armando Carlone (nl) Armando Carlone (ast)
LinkedIn personal profile ID	wds:Q57519645-AED2AEAA-9E3D-4403-AB80-77337EFB4B2A
LinkedIn personal profile ID	armandocarlone
Scopus author ID	wds:Q57519645-E9803CAF-AAEE-41BD-852D-EBC8547B0A37
Scopus author ID	6506442087
given name	wds:Q57519645-7AF15B99-AE67-4A2C-B7A9-D062144F168A
given name	Armando
instance of	wds:Q57519645-72210BD3-E37A-4978-B9FD-DC4F69622011
instance of	Homo sapiens
occupation	wds:Q57519645-FCA67683-B825-4373-A578-79C78160D9B9
employer	wds:Q57519645-5E5CAAF0-61A2-4337-B5CF-59F25EE12BF5 wds:Q57519645-D7A43BEB-C806-40E9-9ED7-E105F23CEBD2
sex or gender	wds:Q57519645-6243602A-F6F5-4A7A-BAD7-D03192103103
educated at	wds:Q57519645-1B44AFCB-6278-448E-93DE-CC1AB9B1CB54 wds:Q57519645-BADF1D10-E5B5-4A61-A69D-C2F48724B0CD
family name	wds:Q57519645-D8B57658-65FF-4494-BAF7-E2D88274A786
occupation	researcher
employer	University of L'Aquila University of Edinburgh
sex or gender	male
educated at	University of Bologna University of L'Aquila
family name	Carlone
ORCID iD	wds:Q57519645-2920287F-318F-4C44-A00C-1F630C8043FF
ORCID iD	https://orcid.org/0000-0003-2983-6445
ORCID iD	0000-0003-2983-6445
IRIS UNIBO author ID	wds:Q57519645-2555832F-8D7C-42FF-89F6-06D1C5D5F34B
IRIS UNIBO author ID	11806
IRIS UNIVAQ author ID	wds:Q57519645-4AA6474B-827D-4BAA-BD8A-AA403F22F522
IRIS UNIVAQ author ID	24369
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57519645
is author of	Organocatalytic asymmetric Friedel-Crafts alkylation of indoles with simple alpha,beta-unsaturated ketones A Three-Compartment Chemically-Driven Molecular Information Ratchet A small molecule that walks non-directionally along a track without external intervention A New Approach for an Organocatalytic Multicomponent Domino Asymmetric Reaction An autonomous chemically fuelled small-molecule motor Aminocatalytic enantioselective anti-Mannich reaction of aldehydes with in situ generated N-Cbz and N-Boc imines Asymmetric aminocatalysis--gold rush in organic chemistry Asymmetric aminolysis of aromatic epoxides: a facile catalytic enantioselective synthesis of anti-beta-amino alcohols Quaternary stereogenic carbon atoms in complex molecules by an asymmetric, organocatalytic, triple-cascade reaction A Rotaxane-Based Switchable Organocatalyst Organocatalytic asymmetric alpha-selenenylation of aldehydes A simple asymmetric organocatalytic approach to optically active cyclohexenones Organocatalytic asymmetric hydrophosphination of alpha,beta-unsaturated aldehydes Organocatalytic asymmetric conjugate addition of 1,3-dicarbonyl compounds to maleimides Alcohols and di-tert-butyl dicarbonate: how the nature of the Lewis acid catalyst may address the reaction to the synthesis of tert-butyl ethers Organocatalytic asymmetric alpha-halogenation of 1,3-dicarbonyl compounds Influence of structurally related micelle forming surfactants on the antioxidant activity of natural substances Iridium(III) Complexes with Fluorinated Phenyl-tetrazoles as Cyclometalating Ligands: Enhanced Excited-State Energy and Blue Emission Asymmetric catalytic synthesis of enantiopure N-protected 1,2-amino alcohols Direct catalytic synthesis of enantiopure 5-substituted oxazolidinones from racemic terminal epoxides Organocatalytic asymmetric hydrophosphination of nitroalkenes Organocatalytic Asymmetric Conjugate Additions to Cyclopent-1-enecarbaldehyde: A Critical Assessment of Organocatalytic Approaches towards the Telaprevir Bicyclic Core Kinetic resolution of oxazinones: rational exploration of chemical space through the design of experiments Palladium-catalyzed regio- and stereoselective synthesis of aryl and 3-indolyl-substituted 4-methylene-3,4-dihydroisoquinolin-1(2H)-ones
is author of	wds:Q56993717-CB3B4C08-B08E-4436-AB05-8512B6FAE049 wds:Q93165676-F92AFDF3-042C-40B6-A4D5-32B4AB56261F wds:Q101126172-199AE1C2-F9B9-4103-B7DE-FA3988B7A692 wds:Q56999378-00296D75-831E-405A-8707-5A9B2D4E4B55 wds:Q57001232-FBABA725-AC23-43E4-B9F9-69223F160D4A wds:Q81083977-8B2FF74D-14A8-4FE0-AAF6-9706DD0CB43A wds:Q56996088-52B9939F-A41A-49FD-B652-F315CB16A31A wds:Q57001760-89BBA5B8-7A1E-4E5C-BA0C-22B8263A530B wds:Q80752471-922BD0A1-9E51-438A-9DFC-FC65A8CDD8DE wds:Q29011653-24538082-00EC-4A98-BB9A-5290EED32C8D wds:Q34226455-3633549C-F238-45A1-B21C-FB4E6F8CC26E wds:Q56996648-9F6568CD-1AE5-40FB-B251-631DB60826E1 wds:Q56999957-07E7B7E3-0166-438B-9A5B-89113EBD4A18 wds:Q56967107-232B27E5-9E06-465C-AC1C-88842CD5CEBC wds:Q57384139-6123773D-C825-4329-A75A-48523E2AB126 wds:Q57384140-53C7B970-E382-4EC9-B0A2-2D0BCE5F0E95 wds:Q79394458-A338DA82-5AE7-48F8-8E45-247CEDA41A4D wds:Q56995579-C76CDEC2-7424-4CF5-B180-6DFF7EEFAD32 wds:Q37230100-3B8B0A88-F9ED-4C3D-ABFF-F3E266C27954 wds:Q62023085-D837DBF4-2C85-4BF4-A853-169DF18D8F6B

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