Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 64 checked references that resolve
resolves10.1039/b920163gRecent developments in carbon dioxide utilization under mild conditions
resolves10.1039/b700658fUtilisation of CO2 as a chemical feedstock: opportunities and challenges
resolves10.1021/cr000018sCatalysis Research of Relevance to Carbon Management: Progress, Challenges, and Opportunities
resolves10.1039/B614037HInsertion of CO
<sub>2</sub>
into a palladiumallyl bond and a Pd(
<scp>ii</scp>
) catalysed carboxylation of allyl stannanes
resolves10.1021/ol800764uNickel-Catalyzed Carboxylation of Organozinc Reagents with CO<sub>2</sub>
resolves10.1021/ja803435wBeyond Aresta’s Complex: Ni- and Pd-Catalyzed Organozinc Coupling with CO<sub>2</sub>
resolves10.1021/ja061232mRhodium(I)-Catalyzed Carboxylation of Aryl- and Alkenylboronic Esters with CO<sub>2</sub>
resolves10.1021/ol800829qCopper(I)-Catalyzed Carboxylation of Aryl- and Alkenylboronic Esters
resolves10.1002/anie.200801857Carboxylation of Organoboronic Esters Catalyzed by N‐Heterocyclic Carbene Copper(I) Complexes
resolves10.1002/anie.200504024Mixed Mg/Li Amides of the Type R<sub>2</sub>NMgCl⋅LiCl as Highly Efficient Bases for the Regioselective Generation of Functionalized Aryl and Heteroaryl Magnesium Compounds
resolves10.1039/b704362gStructurally-defined direct C-magnesiation and C-zincation of N-heterocyclic aromatic compounds using alkali-metal-mediated metallation
resolves10.1021/ja064601nAn Aluminum Ate Base: Its Design, Structure, Function, and Reaction Mechanism
resolves10.1002/anie.200701984(tmp)<sub>2</sub>Zn⋅2 MgCl<sub>2</sub>⋅2 LiCl: A Chemoselective Base for the Directed Zincation of Sensitive Arenes and Heteroarenes
resolves10.1021/jo100884uRegio- and Chemoselective Zincation of Sensitive and Moderately Activated Aromatics and Heteroaromatics Using TMPZnCl·LiCl
resolves10.1021/ja074669iDirect <i>ortho</i> Cupration: A New Route to Regioselectively Functionalized Aromatics
resolves10.1002/anie.200454084A LiCl‐Mediated Br/Mg Exchange Reaction for the Preparation of Functionalized Aryl‐ and Heteroarylmagnesium Compounds from Organic Bromides
resolves10.1002/anie.200801968Convenient Preparation of Polyfunctional Aryl Magnesium Reagents by a Direct Magnesium Insertion in the Presence of LiCl
resolves10.1038/nchem.590Preparation of functionalized organoaluminiums by direct insertion of aluminium to unsaturated halides
resolves10.1002/anie.200601450Efficient Synthesis of Functionalized Organozinc Compounds by the Direct Insertion of Zinc into Organic Iodides and Bromides
resolves10.1002/anie.200802292Preparation of Aryl and Heteroaryl Indium(III) Reagents by the Direct Insertion of Indium in the Presence of LiCl
resolves10.1021/ol900528hTransition-Metal-Free Carboxylation of Organozinc Reagents Using CO<sub>2</sub>in DMF Solvent
resolves10.1021/jo982443fNickel-Mediated Regio- and Chemoselective Carboxylation of Alkynes in the Presence of Carbon Dioxide
resolves10.1039/b411802bBidentate amidine ligands for nickel(0)-mediated coupling of carbon dioxide with unsaturated hydrocarbons
resolves10.1021/ja8062925Nickel-Catalyzed Reductive Carboxylation of Styrenes Using CO<sub>2</sub>
resolves10.1021/ja806677wHydrocarboxylation of Allenes with CO<sub>2</sub> Catalyzed by Silyl Pincer-Type Palladium Complex
resolves10.1021/ol016585zNickel-Promoted Alkylative or Arylative Carboxylation of Alkynes
resolves10.1021/ol047912gNickel-Catalyzed Regioselective Synthesis of Tetrasubstituted Alkene Using Alkylative Carboxylation of Disubstituted Alkyne
resolves10.1021/ja004004fCross-Coupling Reaction of Oxo-π-allylnickel Complex Generated from 1,3-Diene under an Atmosphere of Carbon Dioxide
resolves10.1246/cl.2002.102Lewis Acid-Mediated Carboxylation of Fused Aromatic Compounds with Carbon Dioxide
resolves10.1021/ja020787oEfficient Chemoselective Carboxylation of Aromatics to Arylcarboxylic Acids with a Superelectrophilically Activated Carbon Dioxide−Al<sub>2</sub>Cl<sub>6</sub>/Al System
resolves10.1021/ie801524eEffect of Incubation of CO<sub>2</sub> and Lewis Acid on the Generation of Toluic Acid from Toluene and CO<sub>2</sub>
resolves10.1016/S0040-4039(00)78044-0Syntheses of γ,δ-unsaturated alcohols from allylsilanes and carbonyl compounds in the presence of titanium tetrachloride
resolves10.1246/cl.2003.454Lewis Acid-Mediated Carboxylation of Aryl- and Allylsilanes with Carbon Dioxide
resolves10.1246/cl.2006.820Beneficial Effect of TMSCl in the Lewis Acid-mediated Carboxylation of Aromatic Compounds with Carbon Dioxide
resolves10.1021/ja00216a032Friedel-Crafts chemistry. 11. Boron, aluminum, and gallium tris(trifluoromethanesulfonate) (triflate): effective new Friedel-Crafts catalysts
resolves10.1021/cr00078a005Dehydro coupling of aromatic nuclei by catalyst-oxidant systems: poly(p-phenylene)
resolves10.1021/ja00764a040Acid-catalyzed isomerization of 1,2-bis(trimethylsilyl)benzene and related compounds
resolves10.1021/ja00995a048Silylation of ferrocene by chloro- and aminosilanes under Friedel-Crafts conditions
resolves10.1021/jo00277a005Aromatic substitution. 56. Observation of aluminum trichloride-catalyzed trialkylsilylation of benzene and toluene with chlorotrialkylsilanes in the presence of Huenig bases
resolves10.1021/ja906566rDevelopment of a Sila-Friedel−Crafts Reaction and Its Application to the Synthesis of Dibenzosilole Derivatives
resolves10.1002/hlca.19570400324Etude spectrographique des complexes formés par les halogénures d'aluminium et le trifluorure de bore. III – Spectre d'absorption infrarouge et pression de vapeur du composé d'addition des fluorures de bore et d'acétyle
resolves10.1002/hlca.19570400412Etude spectroscopique des complexes formés par les acides de <i>Lewis</i>. IV. Spectre d'absorption infrarouge des composés d'addition du chlorure d'aluminium avec les chlorures d'acétyle et de mésitoyle
resolves10.1002/hlca.19610440208Etudes de composés d'addition des acides de L<scp>EWIS</scp> XIII. Composés d'addition de chlorures de benzoyle orthosubstitués avec TiCl<sub>4</sub> et AlCl<sub>3</sub>
resolves10.3891/acta.chem.scand.20-1351Stereochemistry of a Friedel-Crafts Intermediate. The Crystal Structure of the Aluminiumchloride-Benzoyl Chloride Complex.
resolves10.1107/S0567740872004406Etude de complexes acide de Lewis–halogénure d'acide. I. Structure cristalline des hexachloroantimonate, tétrachloroaluminate et tétrachlorogallate de méthyl oxocarbonium
resolves10.1055/s-1988-27549One-Pot Syntheses of Methyl<i>p</i>- and<i>o</i>-Hydroxydithiobenzoates from Phenol Ethers
resolves10.1081/SIM-100105262SYNTHESES AND CHARACTERIZATION OF ALUMINIUM(III), IRON(III), AND COPPER(II) MONOBROMOACETATES AND THEIR COMPLEXES WITH ORGANIC BASES
resolves10.1021/ol802837mRegiocontrolled Cobalt-Catalyzed Diels−Alder Reactions of Silicon-Functionalized, Terminal, and Internal Alkynes
resolves10.1021/jo01294a032Reactions of .beta.-diketones with aromatic aldehydes and ketones in the presence of potassium hydride
The 10 references without a DOI — listed, not checked
no DOI — not checkedReviews:
no DOI — not checkedref19/cit19a
no DOI — not checkedref19/cit19c
no DOI — not checkedref19/cit19d
no DOI — not checkedfHuesler, R.; Orban, I.; Holer, M.Eur. Pat. Appl. 1996, EP 706987.
no DOI — not checkedref23/cit23a
no DOI — not checkedref32/cit32
no DOI — not checkedFor the X ray structures of acyl halide−AlCl3complexes, see:
no DOI — not checkedFor Friedel-Crafts-type dithiocarboxylation, see:
no DOI — not checkedref37/cit37a
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