At the dated check, the references listed below either did not resolve in
Crossref or DataCite, or carried a retraction notice. Each one is shown with the
registry record that put it there.
The 57 checked references that resolve
resolves10.1021/cr0684319Gold-Catalyzed Cycloisomerizations of Enynes: A Mechanistic Perspective
resolves10.1039/b807499mCarbocyclisation of alkynes with external nucleophiles catalysed by gold, platinum and other electrophilic metals
resolves10.1039/b816696jGold and platinum catalysis—a convenient tool for generating molecular complexity
resolves10.1021/cr100376wTransition Metal Catalyzed Cycloisomerizations of 1,
<i>n</i>
-Allenynes and -Allenenes
resolves10.1021/cr1004088Gold-Catalyzed Nucleophilic Cyclization of Functionalized Allenes: A Powerful Access to Carbo- and Heterocycles
resolves10.1039/C0CS00041HGold-catalyzed decorations of arenes and heteroarenes with C–C multiple bonds
resolves10.1039/C2CS15295AStrained small rings in gold-catalyzed rapid chemical transformations
resolves10.1021/cs300043wGold-Containing and Gold-Generated 1,<i>n</i>-Dipoles as Useful Platforms toward Cycloadditions and Cyclizations
resolves10.3762/bjoc.9.261Synthesis of axially chiral gold complexes and their applications in asymmetric catalyses
resolves10.1002/ange.201200739Monomere lineare Diaminocarben‐Gold(I)‐Komplexe in der enantioselektiven Katalyse
resolves10.1002/anie.201200739Monomeric Linear Diaminocarbene Complexes of Gold(I) Show Merit in Enantioselective Catalysis
resolves10.1039/c2sc20542dCatalytic enantioselective carbon-carbon bond formation using cycloisomerization reactions
resolves10.1039/c2cs35020cEnantioselective, transition metal catalyzed cycloisomerizations
resolves10.1039/c1sc00160dEnantioselective synthesis of cyclic carbamimidates via a three-component reaction of imines, terminal alkynes, and p-toluenesulfonylisocyanate using a monophosphine gold(i) catalyst
resolves10.1021/om0491645Ligand Effects in Gold- and Platinum-Catalyzed Cyclization of Enynes: Chiral Gold Complexes for Enantioselective Alkoxycyclization
resolves10.1021/ja068819lGold(I)-Catalyzed Enantioselective Intramolecular Hydroamination of Allenes
resolves10.1002/ange.201003136Diastereo‐ and Enantioselective Gold(I)‐Catalyzed Intermolecular Tandem Cyclization/[3+3]Cycloadditions of 2‐(1‐Alkynyl)‐2‐alken‐1‐ones with Nitrones
resolves10.1002/anie.201003136Diastereo‐ and Enantioselective Gold(I)‐Catalyzed Intermolecular Tandem Cyclization/[3+3]Cycloadditions of 2‐(1‐Alkynyl)‐2‐alken‐1‐ones with Nitrones
resolves10.1002/chem.201100019Enantioselective Gold‐Catalyzed Functionalization of Unreactive sp<sup>3</sup> CH Bonds through a Redox–Neutral Domino Reaction
resolves10.1021/ja103544pGold(I)-Catalyzed Enantioselective Polycyclization Reactions
resolves10.1002/ange.201203507Intermolecular Gold‐Catalyzed Diastereo‐ and Enantioselective [2+2+3] Cycloadditions of 1,6‐Enynes with Nitrones
resolves10.1002/anie.201203507Intermolecular Gold‐Catalyzed Diastereo‐ and Enantioselective [2+2+3] Cycloadditions of 1,6‐Enynes with Nitrones
resolves10.1021/ja304506gGold(I)-Catalyzed Asymmetric Cyclopropenation of Internal Alkynes
resolves10.1021/ja407179cEnantioselective Gold(I)-Catalyzed Vinylogous [3 + 2] Cycloaddition between Vinyldiazoacetates and Enol Ethers
resolves10.1021/ja4040895Highly Stereoselective Olefin Cyclopropanation of Diazooxindoles Catalyzed by a <i>C</i><sub>2</sub>-Symmetric Spiroketal Bisphosphine/Au(I) Complex
resolves10.1021/ja905415rGold-Catalyzed [4C+2C] Cycloadditions of Allenedienes, including an Enantioselective Version with New Phosphoramidite-Based Catalysts: Mechanistic Aspects of the Divergence between [4C+3C] and [4C+2C] Pathways
resolves10.1002/ange.200906550Enantioselective Gold Catalysis: Opportunities Provided by Monodentate Phosphoramidite Ligands with an Acyclic TADDOL Backbone
resolves10.1002/anie.200906550Enantioselective Gold Catalysis: Opportunities Provided by Monodentate Phosphoramidite Ligands with an Acyclic TADDOL Backbone
resolves10.1021/ja200084aPhosphoramidite Gold(I)-Catalyzed Diastereo- and Enantioselective Synthesis of 3,4-Substituted Pyrrolidines
resolves10.1002/ange.201206461Intermolecular [2+2] Reaction of <i>N</i>‐Allenylsulfonamides with Vinylarenes: Enantioselective Gold(I)‐Catalyzed Synthesis of Cyclobutane Derivatives
resolves10.1002/anie.201206461Intermolecular [2+2] Reaction of
<i>N</i>
‐Allenylsulfonamides with Vinylarenes: Enantioselective Gold(I)‐Catalyzed Synthesis of Cyclobutane Derivatives
resolves10.1021/ja3110472Chiral Gold Complex-Catalyzed Hetero-Diels–Alder Reaction of Diazenes: Highly Enantioselective and General for Dienes
resolves10.1021/ja205068jChiral (Acyclic Diaminocarbene)Gold(I)-Catalyzed Dynamic Kinetic Asymmetric Transformation of Propargyl Esters
resolves10.1002/ange.201107789Enantioselective Alkynylbenzaldehyde Cyclizations Catalyzed by Chiral Gold(I) Acyclic Diaminocarbene Complexes Containing Weak Au–Arene Interactions
resolves10.1002/anie.201107789Enantioselective Alkynylbenzaldehyde Cyclizations Catalyzed by Chiral Gold(I) Acyclic Diaminocarbene Complexes Containing Weak Au–Arene Interactions
resolves10.1021/ja3065446Axially Chiral Triazoloisoquinolin-3-ylidene Ligands in Gold(I)-Catalyzed Asymmetric Intermolecular (4 + 2) Cycloadditions of Allenamides and Dienes
resolves10.1016/S0040-4020(99)00451-2Asymmetric synthesis of chiral amines by highly diastereoselective 1,2-additions of organometallic reagents to N-tert-butanesulfinyl imines
resolves10.1039/c2cc30309dKinetic resolution of 1-(1-alkynyl)cyclopropyl ketones by gold(i)-catalyzed asymmetric [4+3]cycloaddition with nitrones: scope, mechanism and applications
The 11 references without a DOI — listed, not checked
no DOI — not checked
no DOI — not checked
no DOI — not checkede_1_2_3_21_2
no DOI — not checkede_1_2_3_25_2
no DOI — not checked
no DOI — not checkedY.‐M. Wang A. D. Lackner F. D. Toste Acc. Chem. Res.2014 DOI:; for earlier examples see:
no DOI — not checked
no DOI — not checked
no DOI — not checkede_1_2_3_45_2
no DOI — not checkedFor an alternative strategy for enantioselective gold catalysis that employs N‐heterocyclic carbenes (NHCs) and acyclic diaminocarbenes (ADCs) as chiral ligands see:
no DOI — not checkedCCDC 984098 ((R RS)‐M3) 984099 ((S RS)‐M5) and 987973 ([{(RS)‐M0}AuCl]) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre viawww.ccdc.cam.ac.uk/data_request/cif.
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