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For: Zheng G, Zhou Z, Zhu G, Zhai S, Xu H, Duan X, Yi W, Li X. Rhodium(III)‐Catalyzed Enantio‐ and Diastereoselective C−H Cyclopropylation of N‐Phenoxylsulfonamides: Combined Experimental and Computational Studies. Angew Chem Int Ed 2020;59:2890-6. [DOI: 10.1002/anie.201913794] [Cited by in Crossref: 56] [Cited by in F6Publishing: 58] [Article Influence: 28.0] [Reference Citation Analysis]
Number Citing Articles
1 Hu P, Liu B, Wang F, Mi R, Li X, Li X. A Stereodivergent–Convergent Chiral Induction Mode in Atroposelective Access to Biaryls via Rhodium-Catalyzed C–H Bond Activation. ACS Catal 2022. [DOI: 10.1021/acscatal.2c04292] [Reference Citation Analysis]
2 Sun J, Zheng G. Chiral Cyclopentadienyl Ligand for Asymmetric CH Activation. Handbook of CH‐Functionalization 2022. [DOI: 10.1002/9783527834242.chf0136] [Reference Citation Analysis]
3 Yu R, Cai S, Li C, Fang X. Nickel‐Catalyzed Asymmetric Hydroaryloxy‐ and Hydroalkoxycarbonylation of Cyclopropenes. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202200733] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
4 Wu M, Zhang H, Wang T, Lin S, Guo Z, Gao H, Zhou Z, Yi W. Rh(III)-Catalyzed chemo-, regio- and stereoselective carboamination of sulfonyl allenes with N-phenoxy amides or N-enoxy imides. Chem Commun (Camb) 2022. [PMID: 35904085 DOI: 10.1039/d2cc02982k] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
5 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]
6 Nagireddy A, Kotipalli R, Nanubolu JB, Sridhar Reddy M. Rhodium-Catalyzed Coordination-Assisted Regioselective and Migratory Three-Point Double Annulation of o-Alkenyl Phenols with Tertiary Propargyl Alcohols. Org Lett 2022. [PMID: 35815845 DOI: 10.1021/acs.orglett.2c01819] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Davies C, Shaaban S, Waldmann H. Asymmetric catalysis with chiral cyclopentadienyl complexes to access privileged scaffolds. Trends in Chemistry 2022. [DOI: 10.1016/j.trechm.2022.01.005] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
8 Wu M, Gao H, Xu H, Yi W, Zhou Z. Enantioselective synthesis of indenopyrazolopyrazolones enabled by dual directing groups-assisted and rhodium(III)-catalyzed tandem C-H alkenylation/[3 + 2] stepwise cycloaddition. Chinese Chemical Letters 2022;33:842-6. [DOI: 10.1016/j.cclet.2021.08.004] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
9 Li B, Xu H, Dang Y, Houk KN. Dispersion and Steric Effects on Enantio-/Diastereoselectivities in Synergistic Dual Transition-Metal Catalysis. J Am Chem Soc . [DOI: 10.1021/jacs.1c12664] [Cited by in Crossref: 15] [Cited by in F6Publishing: 18] [Article Influence: 15.0] [Reference Citation Analysis]
10 Xu H, Fang X, Huang W, Xu Z, Li L, Ye F, Cao J, Xu L. Catalytic regio- and stereoselective silicon–carbon bond formations on unsymmetric gem -difluorocyclopropenes by capture of silyl metal species. Org Chem Front . [DOI: 10.1039/d2qo00943a] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
11 Song X, Wang K, Xue L, Yu H, Zhang X, Lee R, Fan X. Coupling partner-dependent unsymmetrical C–H functionalization of N -phenoxyacetamides leading to sophisticated spirocyclic scaffolds. Org Chem Front . [DOI: 10.1039/d2qo00851c] [Reference Citation Analysis]
12 Wei Y, Xu H, Chen F, Gao H, Huang Y, Yi W, Zhou Z. Specific assembly of dihydrobenzofuran frameworks via Rh( iii )-catalysed C–H coupling of N -phenoxyacetamides with 2-alkenylphenols. New J Chem 2022;46:5705-11. [DOI: 10.1039/d2nj00175f] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Liu C, Wang Q, Gu Q, You S. C C Bond Formation Through C-H Activation. Comprehensive Organometallic Chemistry IV 2022. [DOI: 10.1016/b978-0-12-820206-7.00087-1] [Reference Citation Analysis]
14 Xu H, Chen W, Bian M, Xu H, Gao H, Wang T, Zhou Z, Yi W. Gem -Difluorocyclopropenes as Versatile β-Monofluorinated Three-sp 2 Carbon Sources for Cp*Rh(III)-Catalyzed [4 + 3] Annulation: Experimental Development and Mechanistic Insight. ACS Catal 2021;11:14694-701. [DOI: 10.1021/acscatal.1c04508] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 10.0] [Reference Citation Analysis]
15 Zhao F, Zhou Z, Lu Y, Qiao J, Zhang X, Gong X, Liu S, Lin S, Wu X, Yi W. Chemo-, Regio-, and Stereoselective Assembly of Polysubstituted Furan-2(5 H )-ones Enabled by Rh(III)-Catalyzed Domino C–H Alkenylation/Directing Group Migration/Lactonization: A Combined Experimental and Computational Study. ACS Catal 2021;11:13921-34. [DOI: 10.1021/acscatal.1c03846] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 8.0] [Reference Citation Analysis]
16 Rachwalski M, Buchcic-szychowska A, Leśniak S. Recent Advances in Selected Asymmetric Reactions Promoted by Chiral Catalysts: Cyclopropanations, Friedel–Crafts, Mannich, Michael and Other Zinc-Mediated Processes—An Update. Symmetry 2021;13:1762. [DOI: 10.3390/sym13101762] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Chen F, Tang J, Wei Y, Tian J, Gao H, Yi W, Zhou Z. Rh(III)-Catalyzed and synergistic dual directing group-enabled redox-neutral [3+3] annulation of N-phenoxyacetamides with α-allenols. Chem Commun (Camb) 2021;57:9284-7. [PMID: 34519313 DOI: 10.1039/d1cc03206b] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
18 Kim YL, Park SA, Choi SM, Park JU, Kim JH. CoIII-Catalyzed C-H Alkenylation and Allylation with Cyclopropenes via Sequential C-H/C-C Bond Activation. Org Lett 2021;23:6674-9. [PMID: 34474571 DOI: 10.1021/acs.orglett.1c02219] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
19 Zhai Y, Zhang X, Ma S. Stereoselective rhodium-catalyzed 2-C-H 1,3-dienylation of indoles: dual functions of the directing group. Chem Sci 2021;12:11330-7. [PMID: 34667543 DOI: 10.1039/d1sc02167b] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
20 Wang F, Jing J, Zhao Y, Zhu X, Zhang XP, Zhao L, Hu P, Deng WQ, Li X. Rhodium-Catalyzed C-H Activation-Based Construction of Axially and Centrally Chiral Indenes through Two Discrete Insertions. Angew Chem Int Ed Engl 2021;60:16628-33. [PMID: 34008279 DOI: 10.1002/anie.202105093] [Cited by in Crossref: 27] [Cited by in F6Publishing: 30] [Article Influence: 27.0] [Reference Citation Analysis]
21 Xu H, Bian M, Zhou Z, Gao H, Yi W. Mechanistic Insights into the Dual Directing Group-Mediated C-H Functionalization/Annulation via a Hydroxyl Group-Assisted MIII-MV-MIII Pathway. ACS Omega 2021;6:17642-50. [PMID: 34278149 DOI: 10.1021/acsomega.1c02183] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
22 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: 18.0] [Reference Citation Analysis]
23 Wei Y, Jiang X, Gao H, Bian M, Huang Y, Zhou Z, Yi W. Rhodium(III)‐Catalyzed Cascade C−H Coupling/C‐Terminus Michael Addition of N ‐Phenoxy Amides with 1,6‐Enynes. ChemistrySelect 2021;6:6574-6578. [DOI: 10.1002/slct.202102186] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
24 Pan C, Yin SY, Wang SB, Gu Q, You SL. Oxygen-Linked Cyclopentadienyl Rhodium(III) Complexes-Catalyzed Asymmetric C-H Arylation of Benzo[h]quinolines with 1-Diazonaphthoquinones. Angew Chem Int Ed Engl 2021;60:15510-6. [PMID: 33856719 DOI: 10.1002/anie.202103638] [Cited by in Crossref: 39] [Cited by in F6Publishing: 43] [Article Influence: 39.0] [Reference Citation Analysis]
25 Wang F, Jing J, Zhao Y, Zhu X, Zhang X, Zhao L, Hu P, Deng W, Li X. Rhodium‐Catalyzed C−H Activation‐Based Construction of Axially and Centrally Chiral Indenes through Two Discrete Insertions. Angew Chem 2021;133:16764-9. [DOI: 10.1002/ange.202105093] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
26 Pan C, Yin S, Wang S, Gu Q, You S. Oxygen‐Linked Cyclopentadienyl Rhodium(III) Complexes‐Catalyzed Asymmetric C−H Arylation of Benzo[ h ]quinolines with 1‐Diazonaphthoquinones. Angew Chem 2021;133:15638-44. [DOI: 10.1002/ange.202103638] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 12.0] [Reference Citation Analysis]
27 Zhang H, Lin S, Gao H, Zhang K, Wang Y, Zhou Z, Yi W. Chemodivergent assembly of ortho-functionalized phenols with tunable selectivity via rhodium(III)-catalyzed and solvent-controlled C-H activation. Commun Chem 2021;4. [DOI: 10.1038/s42004-021-00518-x] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
28 Mi R, Zhang X, Wang J, Chen H, Lan Y, Wang F, Li X. Rhodium-Catalyzed Regio-, Diastereo-, and Enantioselective Three-Component Carboamination of Dienes via C–H Activation. ACS Catal 2021;11:6692-7. [DOI: 10.1021/acscatal.1c01615] [Cited by in Crossref: 12] [Cited by in F6Publishing: 14] [Article Influence: 12.0] [Reference Citation Analysis]
29 Nie S, Lu A, Kuker EL, Dong VM. Enantioselective Hydrothiolation: Diverging Cyclopropenes through Ligand Control. J Am Chem Soc 2021;143:6176-84. [PMID: 33856804 DOI: 10.1021/jacs.1c00939] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 16.0] [Reference Citation Analysis]
30 Wu L, Li L, Zhang H, Gao H, Zhou Z, Yi W. Rh(III)-Catalyzed C-H Activation/[3 + 2] Annulation of N-Phenoxyacetamides via Carbooxygenation of 1,3-Dienes. Org Lett 2021;23:3844-9. [PMID: 33870686 DOI: 10.1021/acs.orglett.1c00945] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
31 Zhong X, Lin S, Gao H, Liu FX, Zhou Z, Yi W. Rh(III)-Catalyzed Redox-Neutral C-H Activation/[3 + 2] Annulation of N-Phenoxy Amides with Propargylic Monofluoroalkynes. Org Lett 2021;23:2285-91. [PMID: 33657804 DOI: 10.1021/acs.orglett.1c00418] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 8.0] [Reference Citation Analysis]
32 Wu L, Xu H, Gao H, Li L, Chen W, Zhou Z, Yi W. Chiral Allylic Amine Synthesis Enabled by the Enantioselective Cp X Rh(III)-Catalyzed Carboaminations of 1,3-Dienes. ACS Catal 2021;11:2279-87. [DOI: 10.1021/acscatal.0c04777] [Cited by in Crossref: 17] [Cited by in F6Publishing: 20] [Article Influence: 17.0] [Reference Citation Analysis]
33 Chen K, Chen W, Chen F, Zhang H, Xu H, Zhou Z, Yi W. Synthesis of 2-aminobenzofurans via base-mediated [3 + 2] annulation of N -phenoxy amides with gem -difluoroalkenes. Org Chem Front 2021;8:4452-8. [DOI: 10.1039/d1qo00709b] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 6.0] [Reference Citation Analysis]
34 Meng H, Yang F, Chen M, Chen C, Zhu B. Rh( iii )-Catalyzed switchable C–H monoalkenylation and dialkenylation of 2-(1 H -pyrazol-1-yl)pyridine with alkenes via rollover cyclometalation. Org Chem Front 2021;8:773-7. [DOI: 10.1039/d0qo01325k] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
35 Xie H, Zhong M, Wang X, Wu J, Cai Y, Liu J, Shu B, Che T, Zhang S. Cp*Ir( iii )- and Cp*Rh( iii )-catalyzed C(sp 2 )–H amination of arenes using thioethers as directing groups. Org Chem Front 2021;8:635-42. [DOI: 10.1039/d0qo01353f] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 16.0] [Reference Citation Analysis]
36 Zhang J, Xu Q, Fan J, Zhou L, Liu N, Zhu L, Wu J, Xie M. Pd( ii )-Catalyzed enantioconvergent twofold C–H annulation to access atropisomeric aldehydes: a platform for diversity-oriented-synthesis. Org Chem Front 2021;8:3404-12. [DOI: 10.1039/d1qo00183c] [Cited by in Crossref: 10] [Cited by in F6Publishing: 12] [Article Influence: 10.0] [Reference Citation Analysis]
37 Bian M, Mawjuda H, Gao H, Xu H, Zhou Z, Yi W. Lossen Rearrangement vs C-N Reductive Elimination Enabled by Rh(III)-Catalyzed C-H Activation/Selective Lactone Ring-Opening: Chemodivergent Synthesis of Quinolinones and Dihydroisoquinolinones. Org Lett 2020;22:9677-82. [PMID: 33274634 DOI: 10.1021/acs.orglett.0c03734] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
38 Zhu Y, Chen F, Cheng D, Chen Y, Zhao X, Wei W, Lu Y, Zhao J. Rhodium(III)-Catalyzed Alkenyl C-H Functionalization to Dienes and Allenes. Org Lett 2020;22:8786-90. [PMID: 33147030 DOI: 10.1021/acs.orglett.0c03126] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
39 Kou L, Dai P, Bao X. Mechanistic Insights into the Rh(I)/Rh 2 (II)‐Catalyzed Divergent Ring‐Opening of Cyclopropenes: A Computational Study. ChemCatChem 2020;12:5656-63. [DOI: 10.1002/cctc.202001149] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
40 Mas‐roselló J, Herraiz AG, Audic B, Laverny A, Cramer N. Chiral Cyclopentadienyl Ligands: Design, Syntheses, and Applications in Asymmetric Catalysis. Angew Chem 2021;133:13306-32. [DOI: 10.1002/ange.202008166] [Cited by in Crossref: 33] [Cited by in F6Publishing: 33] [Article Influence: 16.5] [Reference Citation Analysis]
41 Mas‐roselló J, Herraiz AG, Audic B, Laverny A, Cramer N. Chiral Cyclopentadienyl Ligands: Design, Syntheses, and Applications in Asymmetric Catalysis. Angew Chem Int Ed 2021;60:13198-224. [DOI: 10.1002/anie.202008166] [Cited by in Crossref: 97] [Cited by in F6Publishing: 104] [Article Influence: 48.5] [Reference Citation Analysis]
42 Zhang Y, Li Y, Zhou W, Zhang M, Zhang Q, Jia R, Zhao J. Assembly of polysubstituted chiral cyclopropylamines via highly enantioselective Cu-catalyzed three-component cyclopropene alkenylamination. Chem Commun (Camb) 2020;56:12250-3. [PMID: 32929423 DOI: 10.1039/d0cc01060j] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
43 Liang H, Vasamsetty L, Li T, Jiang J, Pang X, Wang J. A New Class of C2 -Symmetric Chiral Cyclopentadienyl Ligand Derived from Ferrocene Scaffold: Design, Synthesis and Application. Chemistry 2020;26:14546-50. [PMID: 32470226 DOI: 10.1002/chem.202001814] [Cited by in Crossref: 21] [Cited by in F6Publishing: 24] [Article Influence: 10.5] [Reference Citation Analysis]
44 Li G, Yan X, Jiang J, Liang H, Zhou C, Wang J. Chiral Bicyclo[2.2.2]octane-Fused CpRh Complexes: Synthesis and Potential Use in Asymmetric C-H Activation. Angew Chem Int Ed Engl 2020;59:22436-40. [PMID: 32840946 DOI: 10.1002/anie.202010489] [Cited by in Crossref: 26] [Cited by in F6Publishing: 31] [Article Influence: 13.0] [Reference Citation Analysis]
45 Li G, Yan X, Jiang J, Liang H, Zhou C, Wang J. Chiral Bicyclo[2.2.2]octane‐Fused CpRh Complexes: Synthesis and Potential Use in Asymmetric C−H Activation. Angew Chem 2020;132:22622-6. [DOI: 10.1002/ange.202010489] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 4.5] [Reference Citation Analysis]
46 Sun J, Yuan W, Tian R, Wang P, Zhang X, Li X. Rhodium(III)‐Catalyzed Asymmetric [4+1] and [5+1] Annulation of Arenes and 1,3‐Enynes: A Distinct Mechanism of Allyl Formation and Allyl Functionalization. Angew Chem 2020;132:22895-902. [DOI: 10.1002/ange.202010832] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
47 Sun J, Yuan W, Tian R, Wang P, Zhang X, Li X. Rhodium(III)‐Catalyzed Asymmetric [4+1] and [5+1] Annulation of Arenes and 1,3‐Enynes: A Distinct Mechanism of Allyl Formation and Allyl Functionalization. Angew Chem Int Ed 2020;59:22706-13. [DOI: 10.1002/anie.202010832] [Cited by in Crossref: 23] [Cited by in F6Publishing: 26] [Article Influence: 11.5] [Reference Citation Analysis]
48 Yang Y, Zhang K, Yang J, Zhu G, Chen W, Zhang C, Zhou Z, Yi W. Ru(II)-Catalyzed and acidity-controlled tunable [5+1]/[5+2] annulation for building ring-fused quinazolines and 1,3-benzodiazepines. Chem Commun (Camb) 2020;56:11315-8. [PMID: 32840534 DOI: 10.1039/d0cc04041j] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 4.5] [Reference Citation Analysis]
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51 Wang F, Qi Z, Zhao Y, Zhai S, Zheng G, Mi R, Huang Z, Zhu X, He X, Li X. Rhodium(III)‐Catalyzed Atroposelective Synthesis of Biaryls by C−H Activation and Intermolecular Coupling with Sterically Hindered Alkynes. Angew Chem 2020;132:13390-6. [DOI: 10.1002/ange.202002208] [Cited by in Crossref: 26] [Cited by in F6Publishing: 26] [Article Influence: 13.0] [Reference Citation Analysis]
52 Wang F, Qi Z, Zhao Y, Zhai S, Zheng G, Mi R, Huang Z, Zhu X, He X, Li X. Rhodium(III)‐Catalyzed Atroposelective Synthesis of Biaryls by C−H Activation and Intermolecular Coupling with Sterically Hindered Alkynes. Angew Chem Int Ed 2020;59:13288-94. [DOI: 10.1002/anie.202002208] [Cited by in Crossref: 74] [Cited by in F6Publishing: 76] [Article Influence: 37.0] [Reference Citation Analysis]
53 Xu H, Gu Y, Zhang S, Xiong H, Ma F, Lu F, Ji Q, Liu L, Ma P, Hou W, Yang G, Lerner RA. A Chemistry for Incorporation of Selenium into DNA‐Encoded Libraries. Angew Chem Int Ed 2020;59:13273-80. [DOI: 10.1002/anie.202003595] [Cited by in Crossref: 26] [Cited by in F6Publishing: 27] [Article Influence: 13.0] [Reference Citation Analysis]
54 Xu H, Gu Y, Zhang S, Xiong H, Ma F, Lu F, Ji Q, Liu L, Ma P, Hou W, Yang G, Lerner RA. A Chemistry for Incorporation of Selenium into DNA‐Encoded Libraries. Angew Chem 2020;132:13375-82. [DOI: 10.1002/ange.202003595] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
55 Wu M, Lin S, Zhu G, Sun M, Zhou Z, Gao H, Yi W. Synergistic Dual Directing Groups-Enabled Diastereoselective C–H Cyclopropylation via Rh(III)-Catalyzed Couplings with Cyclopropenyl Alcohols. Org Lett 2020;22:1295-300. [DOI: 10.1021/acs.orglett.9b04608] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 6.5] [Reference Citation Analysis]
56 Wu S, Wang Z, Ma D, Chen C, Zhu B. Rh( iii )-Catalyzed switchable C–H functionalization of 2-(1 H -pyrazol-1-yl)pyridine with internal alkynes. Org Chem Front 2020;7:1158-63. [DOI: 10.1039/d0qo00248h] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 6.0] [Reference Citation Analysis]