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For: Kang K, Loud NL, DiBenedetto TA, Weix DJ. A General, Multimetallic Cross-Ullmann Biheteroaryl Synthesis from Heteroaryl Halides and Heteroaryl Triflates. J Am Chem Soc 2021;143:21484-91. [PMID: 34918908 DOI: 10.1021/jacs.1c10907] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 6.5] [Reference Citation Analysis]
Number Citing Articles
1 Zhang T, Li R, Hao X, Zhang Q, Yang H, Hou Y, Hou B, Jia L, Jiang K, Zhang Y, Wu X, Zhuang X, Liu L, Yao Y, Guo W, Wang Y. Ullmann-Like Covalent Bond Coupling without Participation of Metal Atoms. ACS Nano 2023;17:4387-95. [PMID: 36802507 DOI: 10.1021/acsnano.2c09467] [Reference Citation Analysis]
2 Ackerman-Biegasiewicz LKG, Kariofillis SK, Weix DJ. Multimetallic-Catalyzed C-C Bond-Forming Reactions: From Serendipity to Strategy. J Am Chem Soc 2023. [PMID: 36913663 DOI: 10.1021/jacs.2c08615] [Reference Citation Analysis]
3 Impastato AC, Brown JTC, Wang Y, Tu NP. Readily Accessible High-Throughput Experimentation: A General Protocol for the Preparation of ChemBeads and EnzyBeads. ACS Med Chem Lett 2023. [DOI: 10.1021/acsmedchemlett.2c00491] [Reference Citation Analysis]
4 Huang X, Tang L, Song Z, Jiang S, Liu X, Ma M, Chen B, Ma Y. Nickel-Catalyzed Desulfonylative Reductive Cross-Coupling of Aryl Sulfones with Aryl Bromides. Org Lett 2023;25:1198-203. [PMID: 36757152 DOI: 10.1021/acs.orglett.3c00185] [Reference Citation Analysis]
5 Taylor CJ, Pomberger A, Felton KC, Grainger R, Barecka M, Chamberlain TW, Bourne RA, Johnson CN, Lapkin AA. A Brief Introduction to Chemical Reaction Optimization. Chem Rev 2023. [PMID: 36820880 DOI: 10.1021/acs.chemrev.2c00798] [Reference Citation Analysis]
6 Li C, Ling L, Luo Z, Wang S, Zhang X, Zeng X. Deoxygenative Cross-Coupling of C(aryl)–O and C(amide)═O Electrophiles Enabled by Chromium Catalysis Using Bipyridine Ligand. ACS Catal 2023. [DOI: 10.1021/acscatal.2c06264] [Reference Citation Analysis]
7 Su ZM, Twilton J, Hoyt CB, Wang F, Stanley L, Mayes HB, Kang K, Weix DJ, Beckham GT, Stahl SS. Ni- and Ni/Pd-Catalyzed Reductive Coupling of Lignin-Derived Aromatics to Access Biobased Plasticizers. ACS Cent Sci 2023;9:159-65. [PMID: 36844489 DOI: 10.1021/acscentsci.2c01324] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Duan A, Xiao F, Lan Y, Niu L. Mechanistic views and computational studies on transition-metal-catalyzed reductive coupling reactions. Chem Soc Rev 2022;51:9986-10015. [PMID: 36374254 DOI: 10.1039/d2cs00371f] [Reference Citation Analysis]
9 Singer RA, Monfette S, Bernhardson D, Tcyrulnikov S, Hubbell AK, Hansen EC. Recent Advances in Nonprecious Metal Catalysis. Org Process Res Dev 2022. [DOI: 10.1021/acs.oprd.2c00310] [Reference Citation Analysis]
10 Qiu J, Xie J, Su S, Gao Y, Meng H, Yang Y, Liao K. Selective functionalization of hindered meta-C–H bond of o-alkylaryl ketones promoted by automation and deep learning. Chem 2022. [DOI: 10.1016/j.chempr.2022.08.015] [Reference Citation Analysis]
11 Salgueiro DC, Chi BK, Guzei IA, García‐reynaga P, Weix DJ. Control of Redox‐Active Ester Reactivity Enables a General Cross‐Electrophile Approach to Access Arylated Strained Rings**. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202205673] [Reference Citation Analysis]
12 Pereira GR, Lopes RP, Wang W, Guimarães T, Teixeira RR, Astruc D. Triazole-functionalized hydrochar-stabilized Pd nanocatalyst for ullmann coupling. Chemosphere 2022. [DOI: 10.1016/j.chemosphere.2022.136250] [Reference Citation Analysis]
13 Song Z, Huang X, Jiang S, He C, Tang L, Ni Q, Ma M, Chen B, Ma Y. C(sp2)-C(sp2) Reductive Cross-Coupling of Triarylphosphines with Aryl Halides by Palladium/Nickel Co-catalysis. Org Lett 2022. [PMID: 35862269 DOI: 10.1021/acs.orglett.2c02139] [Reference Citation Analysis]
14 Jeong J, Jung H, Kim D, Chang S. Multidimensional Screening Accelerates the Discovery of Rhodium Catalyst Systems for Selective Intra- and Intermolecular C–H Amidations. ACS Catal . [DOI: 10.1021/acscatal.2c02612] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Charboneau DJ, Hazari N, Huang H, Uehling MR, Zultanski SL. Homogeneous Organic Electron Donors in Nickel-Catalyzed Reductive Transformations. J Org Chem 2022. [PMID: 35671350 DOI: 10.1021/acs.joc.2c00462] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
16 Cui N, Lin T, Wang YE, Wu J, Han Y, Xu X, Xue F, Xiong D, Walsh PJ, Mao J. Nickel-Catalyzed Reductive Coupling of γ-Metalated Ketones with Unactivated Alkyl Bromides. Org Lett 2022. [PMID: 35639094 DOI: 10.1021/acs.orglett.2c01390] [Reference Citation Analysis]
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