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For: Mato M, Franchino A, Garcı A-Morales C, Echavarren AM. Gold-Catalyzed Synthesis of Small Rings. Chem Rev 2021;121:8613-84. [PMID: 33136374 DOI: 10.1021/acs.chemrev.0c00697] [Cited by in Crossref: 16] [Cited by in F6Publishing: 6] [Article Influence: 8.0] [Reference Citation Analysis]
Number Citing Articles
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7 Stylianakis I, Litinas I, Kolocouris A, Silva López C. Formation and Intramolecular Capture of α-Imino Gold Carbenoids in the Au(I)-Catalyzed [3 + 2] Reaction of Anthranils, 1,2,4-Oxadiazoles, and 4,5-Dihydro-1,2,4-Oxadiazoles with Ynamides. Catalysts 2022;12:915. [DOI: 10.3390/catal12080915] [Reference Citation Analysis]
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9 Fernández-Canelas P, Miguélez R, Rubio E, González JM, Barrio P. Intramolecular activation of strong Si-O bonds by gold(I): regioselective synthesis of 3-bromo-2-silylbenzofurans. Chem Commun (Camb) 2022. [PMID: 35900046 DOI: 10.1039/d2cc03060h] [Reference Citation Analysis]
10 Prakash M, Rani P, Samanta S. A substrate-dependent reaction of 1-aryl-2-alkyl-1,2-diketones with 2-aroyl-1-chlorocyclopropanecarboxylates: selective access to 2',5'-dicyclopropoxy-1,1':4',1''-teraryls and pentafulvenes. Org Biomol Chem 2022. [PMID: 35894220 DOI: 10.1039/d2ob00971d] [Reference Citation Analysis]
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13 Sasane AV, Kuo TC, Cheng MJ, Liu RS. Gold-Catalyzed Rearrangement of α-Carbonyl Cyclopropanes to Form 3-(Cyclopenta-1,3-dien-1-ylmethyl)oxindoles via a Postulated 1,5-Enolate Shift. Org Lett 2022. [PMID: 35816021 DOI: 10.1021/acs.orglett.2c02117] [Reference Citation Analysis]
14 Farshadfar K, Tague AJ, Talebi M, Yates BF, Hyland CJT, Ariafard A. Discovery of Redox-Promoted Brønsted Acid Catalysis in the Gold(III)-Catalyzed Annulation of Phenol and Cyclohexadiene. ACS Catal . [DOI: 10.1021/acscatal.2c01194] [Reference Citation Analysis]
15 Xia J, Liu J, Yu Y, Zhang J, Huang X. Divergent Access to Polycyclic N-Heterocyclic Compounds through Büchner-Type Dearomatization Enabled Cycloisomerization of Diynamides under Gold Catalysis. Org Lett 2022. [PMID: 35666892 DOI: 10.1021/acs.orglett.2c01807] [Reference Citation Analysis]
16 Liu S, Li J, Hu W, Huang B, Cai M. Recyclable gold(I)-catalyzed hydrohydrazidation of terminal alkynes towards keto-N-acylhydrazones. Journal of Organometallic Chemistry 2022. [DOI: 10.1016/j.jorganchem.2022.122411] [Reference Citation Analysis]
17 Pizarro JD, Schmidtke IL, Nova A, Fructos MR, Pérez PJ. Selective Functionalization of Arene C(sp 2 )–H Bonds by Gold Catalysis: The Role of Carbene Substituents. ACS Catal . [DOI: 10.1021/acscatal.2c01713] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
18 Xie D, Xu X, Long S, Tang XY, Wang L. Synthesis of (2-(Quinolin-2-yl)phenyl)carbamates by a One-Pot Friedel-Crafts Reaction/Oxidative Umpolung Aza-Grob Fragmentation Sequence. J Org Chem 2022. [PMID: 35611951 DOI: 10.1021/acs.joc.2c00502] [Reference Citation Analysis]
19 Kumar A, Patil NT. Ligand-Enabled Sustainable Gold Catalysis. ACS Sustainable Chem Eng 2022;10:6900-18. [DOI: 10.1021/acssuschemeng.2c01213] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Fernández-canelas P, Barrio P, González JM. Merging gold catalysis and haloethynyl frames: emphasis on halide-shift processes. Tetrahedron Letters 2022. [DOI: 10.1016/j.tetlet.2022.153857] [Reference Citation Analysis]
21 Gu GH, Lee M, Jung Y, Vlachos DG. Automated exploitation of the big configuration space of large adsorbates on transition metals reveals chemistry feasibility. Nat Commun 2022;13:2087. [PMID: 35474063 DOI: 10.1038/s41467-022-29705-7] [Reference Citation Analysis]
22 Das A, Patil NT. Enantioselective C-H Functionalization Reactions under Gold Catalysis. Chemistry 2022;28:e202104371. [PMID: 35014732 DOI: 10.1002/chem.202104371] [Cited by in Crossref: 2] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
23 Wong ZR, Schramm TK, Loipersberger M, Head‐gordon M, Toste FD. Revisiting the Bonding Model for Gold(I) Species: The Importance of Pauli Repulsion Revealed in a Gold(I)‐Cyclobutadiene Complex. Angewandte Chemie. [DOI: 10.1002/ange.202202019] [Reference Citation Analysis]
24 Fernández S, Santamaría J, Ballesteros A. Lewis Acid Enhancement of Gold Catalytic Activity Through Counterion Coordination. Synthesis of Benzofulvenes from Progargylsilanes and Benzophenones. Adv Synth Catal 2022;364:1286-94. [DOI: 10.1002/adsc.202200165] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
25 Ning Y, Huo M, Wu L, Bi X. Silver-catalyzed cyclopropanation of alkenes with alkynyl N-nosylhydrazones leading to alkynyl cyclopropanes. Chem Commun (Camb) 2022;58:3485-8. [PMID: 35191450 DOI: 10.1039/d2cc00099g] [Reference Citation Analysis]
26 Segura-Quezada LA, Torres-Carbajal KR, Mali N, Patil DB, Luna-Chagolla M, Ortiz-Alvarado R, Tapia-Juárez M, Fraire-Soto I, Araujo-Huitrado JG, Granados-López AJ, Gutiérrez-Hernández R, Reyes-Estrada CA, López-Hernández Y, López JA, Chacón-García L, Solorio-Alvarado CR. Gold(I)-Catalyzed Synthesis of 4H-Benzo[d][1,3]oxazines and Biological Evaluation of Activity in Breast Cancer Cells. ACS Omega 2022;7:6944-55. [PMID: 35252686 DOI: 10.1021/acsomega.1c06637] [Reference Citation Analysis]
27 Hui C, Wang S, Xu C. Dinitrogen extrusion from diazene in organic synthesis. Chinese Chemical Letters 2022. [DOI: 10.1016/j.cclet.2022.03.073] [Reference Citation Analysis]
28 Rodrigalvarez J, Reeve LA, Miró J, Gaunt MJ. Pd(II)-Catalyzed Enantioselective C(sp3)-H Arylation of Cyclopropanes and Cyclobutanes Guided by Tertiary Alkylamines. J Am Chem Soc 2022. [PMID: 35212219 DOI: 10.1021/jacs.1c11921] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
29 Sarmiento JT, Cárcel M, Ramírez de Arellano C, Varea T, Asensio G, Olmos A. Straightforward Synthesis of α-Chloromethylketimines Catalyzed by Gold(I). A Clean Way to Building Blocks. J Org Chem 2022. [PMID: 35191705 DOI: 10.1021/acs.joc.1c02877] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
30 Franchino A, Martí À, Echavarren AM. H-Bonded Counterion-Directed Enantioselective Au(I) Catalysis. J Am Chem Soc 2022. [PMID: 35138843 DOI: 10.1021/jacs.1c11978] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 4.0] [Reference Citation Analysis]
31 Qin H, Zhang H, He P, Wang X, Wu J, Jiang X. Mechanistic studies of carbocycles on elemental mercury adsorption on carbonaceous surface. Fuel 2022;309:122101. [DOI: 10.1016/j.fuel.2021.122101] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
32 Ke J, Lee WC, Wang X, Wang Y, Wen X, Zhang XP. Metalloradical Activation of In Situ-Generated α-Alkynyldiazomethanes for Asymmetric Radical Cyclopropanation of Alkenes. J Am Chem Soc 2022. [PMID: 35099966 DOI: 10.1021/jacs.1c13154] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 5.0] [Reference Citation Analysis]
33 Meng F, Qin X, Li J, Zhang T, Tu S, Jiang B, Hao W. Gold Self‐Relay Catalysis Enabling [3,3]‐Sigmatropic Rearrangement/Nazarov Cyclization and Allylic Alkylation Cascade for Constructing All‐Carbon Quaternary Stereocenters. Chin J Chem . [DOI: 10.1002/cjoc.202100734] [Reference Citation Analysis]
34 Yuan F, Zhao Y, Guo Q, Yin F, Lai J, Nian B, Zhang M, Tang E. Synthesis of 1-[1-(Amino)cyclopropyl]ketones by Tandem Reaction Involving Vinyl Selenium Salt. Chinese Journal of Organic Chemistry 2022;42:1759. [DOI: 10.6023/cjoc202111015] [Reference Citation Analysis]
35 Wang X, Lv R, Li X. Gold( i )-catalyzed diastereo- and enantioselective [4 + 3] cycloadditions: construction of functionalized furano-benzoxepins. Org Chem Front . [DOI: 10.1039/d2qo01070d] [Reference Citation Analysis]
36 Xu Y, Zhai T, Xu Z, Ye L. Recent advances towards organocatalytic enantioselective desymmetrizing reactions. Trends in Chemistry 2022. [DOI: 10.1016/j.trechm.2021.12.010] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
37 Shcherbakov NV, Chikunova EI, Dar'in D, Kukushkin VY, Dubovtsev AY. Redox-Neutral and Atom-Economic Route to β-Carbolines via Gold-Catalyzed [4 + 2] Cycloaddition of Indolylynamides and Cyanamides. J Org Chem 2021;86:17804-15. [PMID: 34812641 DOI: 10.1021/acs.joc.1c02119] [Reference Citation Analysis]
38 Deeprose MJ, Lowe M, Noble A, Booker-Milburn KI, Aggarwal VK. Sequential Photocatalytic Reactions for the Diastereoselective Synthesis of Cyclobutane Scaffolds. Org Lett 2021. [PMID: 34882426 DOI: 10.1021/acs.orglett.1c03746] [Reference Citation Analysis]
39 Hewitt KA, Xie P, Thane TA, Hirbawi N, Zhang S, Matus AC, Lucas EL, Hong X, Jarvo ER. Nickel-Catalyzed Domino Cross-Electrophile Coupling Dicarbofunctionalization Reaction To Afford Vinylcyclopropanes. ACS Catal 2021;11:14369-80. [DOI: 10.1021/acscatal.1c04235] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
40 Senatore R, Malik M, Langer T, Holzer W, Pace V. Consecutive and Selective Double Methylene Insertion of Lithium Carbenoids to Isothiocyanates: A Direct Assembly of Four-Membered Sulfur-Containing Cycles. Angew Chem Int Ed Engl 2021;60:24854-8. [PMID: 34534400 DOI: 10.1002/anie.202110641] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
41 Cheng X, Zhang L. Chiral Bifunctional Phosphine Ligand Enables Gold-Catalyzed Asymmetric Isomerization and Cyclization of Propargyl Sulfonamide into Chiral 3-Pyrroline. Org Lett 2021;23:8194-8. [PMID: 34637317 DOI: 10.1021/acs.orglett.1c02896] [Reference Citation Analysis]
42 Ning X, Chen Y, Hu F, Xia Y. Palladium-Catalyzed Carbene Coupling Reactions of Cyclobutanone N-Sulfonylhydrazones. Org Lett 2021;23:8348-52. [PMID: 34623163 DOI: 10.1021/acs.orglett.1c03052] [Reference Citation Analysis]
43 Cheng PT, Tseng YH, Chein RJ. Organoselenium-Catalyzed Asymmetric Cyclopropanations of (E)-Chalcones. Org Lett 2021;23:8104-8. [PMID: 34612649 DOI: 10.1021/acs.orglett.1c03243] [Reference Citation Analysis]
44 Allegue D, Santamaría J, Ballesteros A. Gold(I)‐Catalyzed Indole Synthesis through Aza‐Nazarov‐Type Cyclization of α‐Imino Gold Carbene Complexes and Arenes. Adv Synth Catal 2021;363:5272-8. [DOI: 10.1002/adsc.202101006] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
45 Shcherbakov NV, Dar'in DV, Kukushkin VY, Dubovtsev AY. Gold-Catalyzed Nitrene Transfer from Benzofuroxans to N-Allylynamides: Synthesis of 3-Azabicyclo[3.1.0]hexanes. J Org Chem 2021;86:12964-72. [PMID: 34472847 DOI: 10.1021/acs.joc.1c01654] [Reference Citation Analysis]
46 Suárez-Rodríguez T, Suárez-Sobrino ÁL, Ballesteros A. Gold(I)-Catalyzed Intermolecular Formal [4+2] Cycloaddition of O-Aryl Ynol Ethers and Enol Ethers: Synthesis of Chromene Derivatives. Chemistry 2021;27:13079-84. [PMID: 34278626 DOI: 10.1002/chem.202102534] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
47 Zuccarello G, Escofet I, Caniparoli U, Echavarren AM. New-Generation Ligand Design for the Gold-Catalyzed Asymmetric Activation of Alkynes. Chempluschem 2021;86:1283-96. [PMID: 34472729 DOI: 10.1002/cplu.202100232] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
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50 Bhoyare VW, Tathe AG, Das A, Chintawar CC, Patil NT. The interplay of carbophilic activation and Au(I)/Au(III) catalysis: an emerging technique for 1,2-difunctionalization of C-C multiple bonds. Chem Soc Rev 2021. [PMID: 34323240 DOI: 10.1039/d0cs00700e] [Reference Citation Analysis]
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54 Shcherbakov NV, Dar’in DV, Kukushkin VY, Dubovtsev AY. Hetero-Tetradehydro-Diels–Alder Cycloaddition of Enynamides and Cyanamides: Gold-Catalyzed Generation of Diversely Substituted 2,6-Diaminopyridines. J Org Chem 2021;86:7218-28. [DOI: 10.1021/acs.joc.1c00558] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
55 Zhang Y, Wei Y, Shi M. A silver-catalyzed domino inverse electron-demand oxo-Diels-Alder reaction of 3-cyclopropylideneprop-2-en-1-ones with 2,3-dioxopyrrolidines via cyclobutane-fused furan. Chem Commun (Camb) 2021;57:3599-602. [PMID: 33710234 DOI: 10.1039/d1cc00707f] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
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