about
A general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagentsCombined experimental and theoretical study on the reductive cleavage of inert C-O bonds with silanes: ruling out a classical Ni(0)/Ni(II) catalytic couple and evidence for Ni(I) intermediates.Ni-catalyzed carboxylation of unactivated primary alkyl bromides and sulfonates with CO2.Remote carboxylation of halogenated aliphatic hydrocarbons with carbon dioxide.Practical Ni-Catalyzed Aryl-Alkyl Cross-Coupling of Secondary Redox-Active Esters.Redox-Active Esters in Fe-Catalyzed C-C Coupling.Metal-catalyzed activation of ethers via C-O bond cleavage: a new strategy for molecular diversity.Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids.Stereodivergent addition of 4-silyloxy-1,2-allenes to aldehydes by hydroboration.Stereocontrolled synthesis of highly functionalized quaternary carbon centers: a route to alpha-substituted serines.Alkyl-(Hetero)Aryl Bond Formation via Decarboxylative Cross-Coupling: A Systematic Analysis.Nickel-catalyzed enantioselective C-C bond formation through C(sp2)-O cleavage in aryl esters.A Highly Reduced Ni‒Li‒Olefin Complex for Catalytic Kumada-Corriu Cross-CouplingsSelective Functionalization of Aminoheterocycles by a Pyrylium SaltThorpe-Ingold Effect in Branch-Selective Alkylation of Unactivated Aryl FluoridesTheortho-Substituent Effect on the Ag-Catalysed Decarboxylation of Benzoic AcidsLigand-Controlled Regiodivergent Ni-Catalyzed Reductive Carboxylation of Allyl Esters with CO2Ni-Catalyzed Stereoselective Arylation of Inert C–O bonds at Low TemperaturesNickel-Catalyzed Decarbonylative CH Coupling Reactions: A Strategy for Preparing Bis(heteroaryl) BackbonesSelective deuteration of (hetero)aromatic compounds via deutero-decarboxylation of carboxylic acidsCarboxylic Acids as Traceless Directing Groups for Formal meta-Selective Direct ArylationIntermolecular Decarboxylative Direct C-3 Arylation of Indoles with Benzoic AcidsSilver-Catalyzed Protodecarboxylation of Heteroaromatic Carboxylic Acids†Selective Late-Stage Sulfonyl Chloride Formation from Sulfonamides Enabled by Pyry-BF4Ni-Catalyzed Reductive Liebeskind-Srogl Alkylation of HeterocyclesBi(I)-Catalyzed Transfer-Hydrogenation with Ammonia-BoraneFluorination of arylboronic esters enabled by bismuth redox catalysisRadical C-N Borylation of Aromatic Amines Enabled by a Pyrylium Reagent
P50
Q28834226-FFBF7C8A-3112-4B0D-9D7D-89F0B61547FBQ30585965-244A6335-4B5F-4DF2-BB07-26A7BACB5215Q33462416-D9D8CC14-8499-4EE0-86FF-54EF7E878D5AQ33470414-8280B5D0-7A73-4142-8B7B-1A3644E7C685Q34511919-B254C525-33B9-48CD-B2CA-26BA3B9184D4Q37243448-C7F0C08D-128C-4410-A2B2-745784A8EF6AQ38243353-87B18B50-C22C-4E63-816E-4060AEB3837CQ41828474-ED9D2F21-5EBE-4BBF-8DFD-996AF30A92D0Q42921551-995525C7-83E7-4396-B0F2-62B6CDF235CBQ46025400-2E6BBCF2-B01A-45C4-B764-399A852814BCQ46420077-2145E489-F192-41F7-9CBB-D8A35FFB7577Q52970074-489BD888-A6BF-4DAA-8C60-63092357BE78Q57284323-1A44B5F5-5848-4E5B-9ADC-A73A729D64F2Q58346997-AA71EBD9-9463-4F09-97F5-D052581A13C8Q58347002-FA6A92D6-A05F-439B-9360-40C04E4C8245Q58347027-4EE661DB-2718-4460-8B00-12037B283EAAQ58347036-93C758E5-114B-4510-AEF7-CAD171E097C8Q58347044-D32FBC62-02D8-4A43-BE72-95D65F203E02Q58347049-992860A0-7577-4913-AFD3-8D5A6DE9B33CQ58347059-9627840F-5C4F-4E1A-AC2D-8AD90783B33BQ58347063-9A93296C-EEC4-43D8-8283-A0953946A313Q58347083-CB3CA1EF-0553-43C9-AB20-7F9C90453BB3Q58347089-9870264D-20AB-4C90-849B-50376A1A221FQ90602213-C824C135-92C0-4AEF-976C-A9813CB029BEQ91076171-92D81123-FACC-4138-A1D0-643D8768DD64Q92000133-47B2C9FA-56EE-4BD3-84B0-0B5C687E7707Q92711194-52E6A33E-7162-45F3-98DE-5D1A137B8232Q93026443-FE4E8EB9-FB87-42D0-B921-8BF9BD035ED2
P50
description
researcher ORCID ID = 0000-0003-4152-7098
@en
wetenschapper
@nl
name
Josep Cornella
@ast
Josep Cornella
@en
Josep Cornella
@es
Josep Cornella
@nl
type
label
Josep Cornella
@ast
Josep Cornella
@en
Josep Cornella
@es
Josep Cornella
@nl
altLabel
Pep
@en
prefLabel
Josep Cornella
@ast
Josep Cornella
@en
Josep Cornella
@es
Josep Cornella
@nl
P106
P21
P31
P496
0000-0003-4152-7098