2 article(s) from Bandini, Marco
Elementary steps in the gold-catalyzed nucleophilic addition to olefins.
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Different approaches for the gold-catalyzed manipulation of inactivated alkenes.
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Computed mechanistic cycle for the gold-catalyzed alkoxylation of ethylene with PhOH.
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[Au(I)]-catalyzed addition of phenols and carboxylic acids to alkenes.
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[Au(III)] catalyzed annulations of phenols and naphthols with dienes.
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[Au(III)]-catalyzed addition of aliphatic alcohols to alkenes.
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[Au(III)]-catalyzed carboalkoxylation of alkenes with dimethyl acetals 6.
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Postulated mechanism for the [Au(I)]-catalyzed hydroamination of olefins.
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Isolation and reactivity of alkyl gold intermediates in the intramolecular hydroamination of alkene...
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[Au(I)]-catalyzed intermolecular hydroamination of dienes.
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Intramolecular [Au(I)]-catalyzed hydroamination of alkenes with carbamates.
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[Au(I)]-catalyzed inter- as well as intramolecular addition of sulfonamides to isolated alkenes.
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Intramolecular hydroamination of N-alkenylureas catalyzed by gold(I) carbene complex.
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Enantioselective hydroamination of alkenyl ureas with biphenyl tropos ligand and chiral silver phos...
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Intramolecular [Au(I)]-catalyzed hydroamination of N-allyl-N’-aryl ureas. (PNP = pNO2-C6H4, PMP = p...
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[Au(I)]-catalyzed hydroamination of alkenes with ammonium salts.
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Enantioselective [Au(I)]-catalyzed intermolecular hydroamination of alkenes with cyclic ureas.
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Mechanistic proposal for the cooperative [Au(I)]/menthol catalysis for the enantioselective intramo...
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[Au(III)]-catalyzed addition of 1,3-diketones to alkenes.
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[Au(I)]-catalyzed intramolecular addition of β-keto amides to alkenes.
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Intermolecular [Au(I)]-catalyzed addition of indoles to alkenes.
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Intermolecular [Au(III)]-catalyzed hydroarylation of alkenes with benzene derivatives and thiophene....
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a) Intramolecular [Au(III)]-catalyzed hydroarylation of alkenes. b) A SEAr-type mechanism was hypot...
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Intramolecular [Au(I)]-catalyzed hydroalkylation of alkenes with simple ketones.
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Proposed reaction mechanism for the intramolecular [Au(I)]-catalyzed hydroalkylation of alkenes wit...
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Tandem Michael addition/hydroalkylation catalyzed by [Au(I)] and [Ag(I)] salts.
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Intramolecular [Au(I)]-catalyzed tandem migration/[2 + 2] cycloaddition of 1,7-enyne benzoates.
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Intramolecular [Au(I)]-catalyzed cyclopropanation of alkenes.
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Stereospecificity in [Au(I)]-catalyzed hydroalkoxylation of allylic alcohols.
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Mechanistic investigation on the intramolecular [Au(I)]-catalyzed hydroalkoxylation of allylic alco...
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Mechanistic investigation on the intramolecular enantioselective [Au(I)]-catalyzed alkylation of in...
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Synthesis of (+)-isoaltholactone via stereospecific intramolecular [Au(I)]-catalyzed alkoxylation o...
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Intramolecular enantioselective dehydrative amination of allylic alcohols catalyzed by chiral [Au(I...
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Enantioselective intramolecular hydroalkylation of allylic alcohols with aldehydes catalyzed by 20c...
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Gold-catalyzed intramolecular diamination of alkenes.
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Gold-catalyzed aminooxygenation and aminoarylation of alkenes.
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Gold-catalyzed carboamination, carboalkoxylation and carbolactonization of terminal alkenes with ar...
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Synthesis of tricyclic indolines via gold-catalyzed formal [3 + 2] cycloaddition.
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Gold(I) catalyzed aminoarylation of terminal alkenes in presence of Selectfluor [dppm = bis(dipheny...
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Mechanistic investigation on the aminoarylation of terminal alkenes by bimetallic gold(I) catalysis...
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Proposed mechanism for the aminoarylation of alkenes via [Au(I)-Au(I)]/[Au(II)-Au(II)] redox cataly...
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Oxyarylation of terminal olefins via redox gold catalysis.
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a) Intramolecular gold-catalyzed oxidative coupling reactions with aryltrimethylsilanes. b) Oxyaryl...
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Oxy- and amino-arylation of alkenes by [Au(I)]/[Au(III)] photoredox catalysis.
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Beilstein J. Org. Chem. 2013, 9, 2586–2614, doi:10.3762/bjoc.9.294
Working hypothesis for the present gold-catalyzed oxaallylic alkylation reaction.
Gold-catalyzed synthesis of γ-lactones 4 from the corresponding monoesters 3.
Mechanistic sketch of the gold-promoted oxaallylic alkylation reaction.
Beilstein J. Org. Chem. 2011, 7, 1198–1204, doi:10.3762/bjoc.7.139
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