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For: Yoshino T, Matsunaga S. Chiral Carboxylic Acid Assisted Enantioselective C–H Activation with Achiral Cp x M III (M = Co, Rh, Ir) Catalysts. ACS Catal 2021;11:6455-66. [DOI: 10.1021/acscatal.1c01351] [Cited by in Crossref: 45] [Cited by in F6Publishing: 52] [Article Influence: 22.5] [Reference Citation Analysis]
Number Citing Articles
1 Shu B, Song JL, Chen SY, Zheng YC, Zhang SS. Rh(III)-Catalyzed C-H Functionalization/Annulation of 1-Arylindazolones: Divergent Synthesis of Fused Indazolones and Allyl Indazolones. J Org Chem 2023;88:3499-508. [PMID: 36891880 DOI: 10.1021/acs.joc.2c02722] [Reference Citation Analysis]
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4 Liang H, Wang J. Enantioselective C-H Bond Functionalization Involving Arene Ruthenium(II) Catalysis. Chemistry 2023;29:e202202461. [PMID: 36300688 DOI: 10.1002/chem.202202461] [Reference Citation Analysis]
5 Zhang WW, Wang Q, Zhang SZ, Zheng C, You SL. (SCp)Rhodium-Catalyzed Asymmetric Satoh-Miura Reaction for Building-up Axial Chirality: Counteranion-Directed Switching of Reaction Pathways. Angew Chem Int Ed Engl 2023;62:e202214460. [PMID: 36383091 DOI: 10.1002/anie.202214460] [Reference Citation Analysis]
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7 Li Y, Liou YC, Oliveira JCA, Ackermann L. Ruthenium(II)/Imidazolidine Carboxylic Acid-Catalyzed C-H Alkylation for Central and Axial Double Enantio-Induction. Angew Chem Int Ed Engl 2022;61:e202212595. [PMID: 36108175 DOI: 10.1002/anie.202212595] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
8 Zeng Z, Gao H, Zhou Z, Yi W. Intermolecular Redox-Neutral Carboamination of C–C Multiple Bonds Initiated by Transition-Metal-Catalyzed C–H Activation. ACS Catal 2022. [DOI: 10.1021/acscatal.2c04964] [Reference Citation Analysis]
9 González JM, Vidal X, Ortuño MA, Mascareñas JL, Gulías M. Chiral Ligands Based on Binaphthyl Scaffolds for Pd-Catalyzed Enantioselective C–H Activation/Cycloaddition Reactions. J Am Chem Soc 2022. [DOI: 10.1021/jacs.2c09479] [Reference Citation Analysis]
10 Qian P, Zhou T, Li J, Zhou Y, Shi B. Ru(II)/Chiral Carboxylic Acid-Catalyzed Asymmetric [4 + 3] Annulation of Sulfoximines with α,β-Unsaturated Ketones. ACS Catal 2022. [DOI: 10.1021/acscatal.2c03531] [Reference Citation Analysis]
11 Whitehurst WG, Kim J, Koenig SG, Chirik PJ. C-H Activation by Isolable Cationic Bis(phosphine) Cobalt(III) Metallacycles. J Am Chem Soc 2022. [PMID: 36194198 DOI: 10.1021/jacs.2c08865] [Reference Citation Analysis]
12 Ma C, Sun Y, Liu S, Li Z, Yang J, Guo H, Zhang J. Enantioselective construction of axially chiral cyclohexylidene scaffolds via Pd-catalyzed asymmetric coupling reaction. Chem Catalysis 2022. [DOI: 10.1016/j.checat.2022.09.025] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
13 Wang Y, Zhang F, Chen H, Li Y, Li J, Ye M. Enantioselective Nickel‐Catalyzed C(sp 3 )−H Activation of Formamides. Angew Chem Int Ed 2022. [DOI: 10.1002/anie.202209625] [Reference Citation Analysis]
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15 Si X, Yang D, Sun M, Wei D, Song M, Niu J. Atroposelective isoquinolinone synthesis through cobalt-catalysed C–H activation and annulation. Nat Synth 2022;1:709-718. [DOI: 10.1038/s44160-022-00114-4] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
16 Yue Q, Liu B, Liao G, Shi B. Binaphthyl Scaffold: A Class of Versatile Structure in Asymmetric C–H Functionalization. ACS Catal . [DOI: 10.1021/acscatal.2c02193] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
17 Li J, Xie P, Zhou T, Qian P, Zhou Y, Li H, Hong X, Shi B. Ir(III)-Catalyzed Asymmetric C–H Activation/Annulation of Sulfoximines Assisted by the Hydrogen-Bonding Interaction. ACS Catal . [DOI: 10.1021/acscatal.2c00962] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
18 Hirata Y, Sekine D, Kato Y, Lin L, Kojima M, Yoshino T, Matsunaga S. Cobalt(III)/Chiral Carboxylic Acid-Catalyzed Enantioselective Synthesis of Benzothiadiazine-1-oxides via C-H Activation. Angew Chem Int Ed Engl 2022;61:e202205341. [PMID: 35491238 DOI: 10.1002/anie.202205341] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
19 Yoshikai N. Cobalt‐Catalyzed Asymmetric CH Functionalization. Handbook of CH‐Functionalization 2022. [DOI: 10.1002/9783527834242.chf0127] [Reference Citation Analysis]
20 Yao QJ, Chen JH, Song H, Huang FR, Shi BF. Cobalt/Salox-Catalyzed Enantioselective C-H Functionalization of Arylphosphinamides. Angew Chem Int Ed Engl 2022;61:e202202892. [PMID: 35385597 DOI: 10.1002/anie.202202892] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 7.0] [Reference Citation Analysis]
21 Hirata Y, Sekine D, Kato Y, Lin L, Kojima M, Yoshino T, Matsunaga S. Cobalt(III)/Chiral Carboxylic Acid‐Catalyzed Enantioselective Synthesis of Benzothiadiazine‐1‐oxides via C−H Activation. Angewandte Chemie. [DOI: 10.1002/ange.202205341] [Reference Citation Analysis]
22 Lv J, Wei Y, Yang L, Yang D, Li H. Different Chiral Ligands Assisted Enantioselective C-H Functionalization with Transition-Metal Catalysts. Catalysts 2022;12:537. [DOI: 10.3390/catal12050537] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
23 Liu YY, Qu YL, Kang YS, Zhu YL, Sun WY, Lu Y. Mild Three-Step Consecutive C-H Activations. Org Lett 2022;24:3118-22. [PMID: 35475650 DOI: 10.1021/acs.orglett.2c00620] [Reference Citation Analysis]
24 Dethe DH, Beeralingappa NC, Siddiqui SA, Chavan PN. Asymmetric Ru/Cinchonine Dual Catalysis for the One-Pot Synthesis of Optically Active Phthalides from Benzoic Acids and Acrylates. J Org Chem 2022. [PMID: 35266689 DOI: 10.1021/acs.joc.1c02961] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
25 Wang Q, Nie Y, Liu C, Zhang W, Wu Z, Gu Q, Zheng C, You S. Rhodium(III)-Catalyzed Enantioselective C–H Activation/Annulation of Ferrocenecarboxamides with Internal Alkynes. ACS Catal 2022;12:3083-93. [DOI: 10.1021/acscatal.2c00083] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
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27 Zhang WW, Liu CX, Yang P, Zhang SZ, Gu Q, You SL. Rhodium-Catalyzed Atroposelective C-H/C-H Cross-Coupling Reaction between 1-Aryl Isoquinoline Derivatives and Indolizines. Org Lett 2022;24:564-9. [PMID: 34985290 DOI: 10.1021/acs.orglett.1c04002] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
28 Xie H, Song JL, Jiang CY, Huang YX, Zeng JY, Liu XG, Zhang SS, Yang F. Thioether-directed Rh(III)-catalyzed peri-selective acyloxylation of arenes. Org Biomol Chem 2022;20:565-9. [PMID: 34985096 DOI: 10.1039/d1ob02236a] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
29 Mi R, Chen H, Zhou X, Li N, Ji D, Wang F, Lan Y, Li X. Rhodium‐Catalyzed Atroposelective Access to Axially Chiral Olefins via C−H Bond Activation and Directing Group Migration. Angewandte Chemie 2022;134. [DOI: 10.1002/ange.202111860] [Reference Citation Analysis]
30 Zheng Y, Shu B, Zeng Y, Chen S, Song J, Liu Y, Xiao L, Liu X, Zhang X, Zhang S. A cascade indazolone-directed Ir( iii )- and Rh( iii )-catalyzed C(sp 2 )–H functionalization/[4 + 2] annulation of 1-arylindazolones with sulfoxonium ylides to access chemically divergent 8 H -indazolo [1,2- a ]cinnolines. Org Chem Front . [DOI: 10.1039/d2qo00871h] [Reference Citation Analysis]
31 Yu X, Zhang Z, Niu J, Shi B. Coordination-assisted, transition-metal-catalyzed enantioselective desymmetric C–H functionalization. Org Chem Front . [DOI: 10.1039/d1qo01884a] [Cited by in Crossref: 11] [Cited by in F6Publishing: 13] [Article Influence: 11.0] [Reference Citation Analysis]
32 Liu Y, Zeng Y, Shu B, Zheng Y, Xiao L, Chen S, Song J, Zhang X, Zhang S. Rh( iii )-Catalyzed dienylation and cyclopropylation of indoles at the C4 position with alkylidenecyclopropanes. Org Chem Front . [DOI: 10.1039/d2qo00763k] [Reference Citation Analysis]
33 Shi Y, Bai W, Mu W, Li J, Yu J, Lian B. Research Progress on Density Functional Theory Study of Palladium-Catalyzed C—H Functionalization to Form C—X (X=O, N, F, I, …) Bonds. Chinese Journal of Organic Chemistry 2022;42:1346. [DOI: 10.6023/cjoc202110027] [Reference Citation Analysis]
34 Fan L, Zhou T, Yang X, Jiang M, Hu X, Shi B. Pd(II)-Catalyzed Enantioselective C—H Olefination of 2-(Arylsulfinyl)pyridines through Kinetic Resolution. Chinese Journal of Organic Chemistry 2022;42:3405. [DOI: 10.6023/cjoc202204058] [Reference Citation Analysis]
35 Jia ZS, Wu YJ, Yao QJ, Xu XT, Zhang K, Shi BF. Pd(II)-Catalyzed Atroposelective C-H Allylation: Synthesis of Enantioenriched N-Aryl Peptoid Atropisomers. Org Lett 2021. [PMID: 34964649 DOI: 10.1021/acs.orglett.1c03967] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
36 Zhang C, Hu X, Dai Y, Yin P, Wang C, Duan W. Asymmetric C–H Activation for the Synthesis of P- and Axially Chiral Biaryl Phosphine Oxides by an Achiral Cp*Ir Catalyst with Chiral Carboxylic Amide. ACS Catal 2022;12:193-9. [DOI: 10.1021/acscatal.1c05080] [Cited by in Crossref: 8] [Cited by in F6Publishing: 11] [Article Influence: 4.0] [Reference Citation Analysis]
37 Hirose J, Wakikawa T, Satake S, Kojima M, Hatano M, Ishihara K, Yoshino T, Matsunaga S. Cp*Rh III /Chiral Disulfonate/CuOAc Catalyst System for the Enantioselective Intramolecular Oxyamination of Alkenes. ACS Catal 2021;11:15187-93. [DOI: 10.1021/acscatal.1c04699] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
38 Zhang Q, Wu L, Shi B. Forging C−heteroatom bonds by transition metal-catalyzed enantioselective C–H functionalization. Chem 2021. [DOI: 10.1016/j.chempr.2021.11.015] [Cited by in Crossref: 21] [Cited by in F6Publishing: 23] [Article Influence: 10.5] [Reference Citation Analysis]
39 Kim Y, Kim D, Chang S. Ir(III)-Catalysed electrooxidative intramolecular dehydrogenative C-H/N-H coupling for the synthesis of N-H indoles. Chem Commun (Camb) 2021;57:12309-12. [PMID: 34734951 DOI: 10.1039/d1cc05882g] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
40 Yang C, Li F, Wu TR, Cui R, Wu BB, Jin RX, Li Y, Wang XS. Development of Axially Chiral Styrene-Type Carboxylic Acid Ligands via Palladium-Catalyzed Asymmetric C-H Alkynylation. Org Lett 2021;23:8132-7. [PMID: 34647750 DOI: 10.1021/acs.orglett.1c02692] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 5.0] [Reference Citation Analysis]
41 Mi R, Chen H, Zhou X, Li N, Ji D, Wang F, Lan Y, Li X. Rhodium-Catalyzed Atroposelective Access to Axially Chiral Olefins via C-H Bond Activation and Directing Group Migration. Angew Chem Int Ed Engl 2021. [PMID: 34677892 DOI: 10.1002/anie.202111860] [Cited by in Crossref: 18] [Cited by in F6Publishing: 20] [Article Influence: 9.0] [Reference Citation Analysis]
42 Yuan WK, Shi BF. Synthesis of Chiral Spirolactams via Sequential C-H Olefination/Asymmetric [4+1] Spirocyclization under a Simple CoII /Chiral Spiro Phosphoric Acid Binary System. Angew Chem Int Ed Engl 2021;60:23187-92. [PMID: 34435722 DOI: 10.1002/anie.202108853] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 9.0] [Reference Citation Analysis]
43 Zhou T, Jiang MX, Qian PF, Yao QJ, Xu XT, Zhang K, Shi BF. Synthesis of Chiral Sulfoxides via Pd(II)-Catalyzed Enantioselective C-H Alkynylation/Kinetic Resolution of 2-(Arylsulfinyl)pyridines. Org Lett 2021;23:7910-5. [PMID: 34605653 DOI: 10.1021/acs.orglett.1c02918] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
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45 Pan C, Yin SY, Gu Q, You SL. CpxM(iii)-catalyzed enantioselective C-H functionalization through migratory insertion of metal-carbenes/nitrenes. Org Biomol Chem 2021;19:7264-75. [PMID: 34612356 DOI: 10.1039/d1ob01248g] [Cited by in Crossref: 9] [Cited by in F6Publishing: 12] [Article Influence: 4.5] [Reference Citation Analysis]
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47 Hu P, Kong L, Wang F, Zhu X, Li X. Twofold C-H Activation-Based Enantio- and Diastereoselective C-H Arylation Using Diarylacetylenes as Rare Arylating Reagents. Angew Chem Int Ed Engl 2021;60:20424-9. [PMID: 34145966 DOI: 10.1002/anie.202106871] [Cited by in Crossref: 22] [Cited by in F6Publishing: 26] [Article Influence: 11.0] [Reference Citation Analysis]
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49 Wang J, Chen H, Kong L, Wang F, Lan Y, Li X. Enantioselective and Diastereoselective C–H Alkylation of Benzamides: Synergized Axial and Central Chirality via a Single Stereodetermining Step. ACS Catal 2021;11:9151-8. [DOI: 10.1021/acscatal.1c02450] [Cited by in Crossref: 18] [Cited by in F6Publishing: 23] [Article Influence: 9.0] [Reference Citation Analysis]
50 Xie H, Liang J, Huang Z, Shu B, Zheng Y, Liu Y, Chen S, Liu X, Zhang S. Rh( iii )-Catalyzed tandem C(sp 2 )–H allylation/ N -alkylation annulation of arene amides with 2-alkylidenetrimethylene carbonates. Org Chem Front 2021;8:6585-90. [DOI: 10.1039/d1qo01129d] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 1.5] [Reference Citation Analysis]
51 Mou Q, Zhao R, Niu R, Fukagawa S, Shigeno T, Yoshino T, Matsunaga S, Sun B. Cp*Ir( iii )/chiral carboxylic acid-catalyzed enantioselective C–H alkylation of ferrocene carboxamides with diazomalonates. Org Chem Front 2021;8:6923-30. [DOI: 10.1039/d1qo01344k] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]