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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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Sheng F, Wang S, Zhou J, Chen C, Wang Y, Zhu S. Control of Axial Chirality through NiH-Catalyzed Atroposelective Hydrofunctionalization of Alkynes. ACS Catal 2023. [DOI: 10.1021/acscatal.2c06200] [Reference Citation Analysis]
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Kim S, Kim A, Lee C, Moon J, Hong EJ, Lee DH, Kwon Y. Atroposelective desymmetrization of 2-arylresorcinols via Tsuji-Trost allylation. Commun Chem 2023;6:42. [PMID: 36841918 DOI: 10.1038/s42004-023-00839-z] [Reference Citation Analysis]
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Chen ZH, Li TZ, Wang NY, Ma XF, Ni SF, Zhang YC, Shi F. Organocatalytic Enantioselective Synthesis of Axially Chiral N,N'-Bisindoles. Angew Chem Int Ed Engl 2023;:e202300419. [PMID: 36749711 DOI: 10.1002/anie.202300419] [Reference Citation Analysis]
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Zhang S, Liu S, Wang X, Wang S, Yang H, Li L, Yang B, Wong MW, Zhao Y, Lu S. Enantioselective Access to Triaryl-2-pyrones with Monoaxial or Contiguous C–C Diaxes via Oxidative NHC Catalysis. ACS Catal 2023. [DOI: 10.1021/acscatal.2c05570] [Reference Citation Analysis]
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Li W, Chen S, Xie J, Fan Z, Yang K, Song Q. Synthesis of axially chiral alkenylboronates through combined copper- and palladium-catalysed atroposelective arylboration of alkynes. Nat Synth 2023. [DOI: 10.1038/s44160-022-00201-6] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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Gong X, Yu N, Gu L, Li Z, Ma W, Zhao F. Redox-neutral rhodium(III)-catalyzed divergent synthesis of tetrasubstituted 1,3-enynes and alkynylated benzofurans. Org Biomol Chem 2022;21:147-52. [PMID: 36465010 DOI: 10.1039/d2ob01800d] [Reference Citation Analysis]
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Wang H, Wu S, Yang J, Zhang Y, Shi F. Design and Organocatalytic Asymmetric Synthesis of Indolyl-Pyrroloindoles Bearing Both Axial and Central Chirality. J Org Chem 2022. [DOI: 10.1021/acs.joc.2c02303] [Reference Citation Analysis]
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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]
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Li Q, Yan K, Zhu Y, Qi G, Wang Y, Hao W, Jiang B. Rh(III)-Catalyzed annulative aldehydic C-H functionalization for accessing ring-fluorinated benzo[b]azepin-5-ones. Chinese Chemical Letters 2022. [DOI: 10.1016/j.cclet.2022.108014] [Reference Citation Analysis]
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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]
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Gou B, Tang Y, Lin Y, Yu L, Jian Q, Sun H, Chen J, Zhou L. Modular Construction of Heterobiaryl Atropisomers and Axially Chiral Styrenes via All‐Carbon Tetrasubstituted VQMs. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202208174] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
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Zhang HH, Shi F. Organocatalytic Atroposelective Synthesis of Indole Derivatives Bearing Axial Chirality: Strategies and Applications. Acc Chem Res 2022;55:2562-80. [PMID: 36053083 DOI: 10.1021/acs.accounts.2c00465] [Cited by in Crossref: 13] [Cited by in F6Publishing: 5] [Article Influence: 13.0] [Reference Citation Analysis]
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Hang Q, Wu S, Yang S, Wang X, Zhong Z, Zhang Y, Shi F. Design and catalytic atroposelective synthesis of axially chiral isochromenone-indoles. Sci China Chem . [DOI: 10.1007/s11426-022-1363-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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Ji D, Jing J, Wang Y, Qi Z, Wang F, Zhang X, Wang Y, Li X. Palladium-catalyzed asymmetric hydrophosphination of internal alkynes: Atroposelective access to phosphine-functionalized olefins. Chem 2022. [DOI: 10.1016/j.chempr.2022.08.019] [Reference Citation Analysis]
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Wu Y, Liu Q, Zhang Q, Ye Z, He Y. Asymmetric allylic substitution-isomerization for accessing axially chiral vinylindoles by intramolecular π … π stacking interactions. Cell Reports Physical Science 2022;3:101005. [DOI: 10.1016/j.xcrp.2022.101005] [Reference Citation Analysis]
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Qin J, Zhou T, Zhou TP, Tang L, Zuo H, Yu H, Wu G, Wu Y, Liao RZ, Zhong F. Catalytic Atroposelective Electrophilic Amination of Indoles. Angew Chem Int Ed Engl 2022;61:e202205159. [PMID: 35612900 DOI: 10.1002/anie.202205159] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
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Wang HW, Wu JX, Huang XQ, Li DC, Wang SN, Lu Y, Dou JM. RhIII-Catalyzed C-H N-Heteroarylation and Esterification Cascade of Carboxylic Acid with Organoboron Reagents and 1,2-Dichloroethane in One-Pot Synthesis. Org Lett 2022. [PMID: 35912970 DOI: 10.1021/acs.orglett.2c02075] [Reference Citation Analysis]
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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]
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Yokose D, Nagashima Y, Kinoshita S, Nogami J, Tanaka K. Enantioselective Synthesis of Axially Chiral Styrene‐Carboxylic Esters by Rhodium‐Catalyzed Chelation‐Controlled [2+2+2] Cycloaddition. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202202542] [Reference Citation Analysis]
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Chen KW, Chen ZH, Yang S, Wu SF, Zhang YC, Shi F. Organocatalytic Atroposelective Synthesis of N-N Axially Chiral Indoles and Pyrroles by De Novo Ring Formation. Angew Chem Int Ed Engl 2022;61:e202116829. [PMID: 35080808 DOI: 10.1002/anie.202116829] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 11.0] [Reference Citation Analysis]
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Yokose D, Nagashima Y, Kinoshita S, Nogami J, Tanaka K. Enantioselective Synthesis of Axially Chiral Styrene‐Carboxylic Esters by Rhodium‐Catalyzed Chelation‐Controlled [2+2+2] Cycloaddition. Angewandte Chemie. [DOI: 10.1002/ange.202202542] [Reference Citation Analysis]
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Wu S, Xiang S, Cheng JK, Tan B. Axially chiral alkenes: Atroposelective synthesis and applications. Tetrahedron Chem 2022;1:100009. [DOI: 10.1016/j.tchem.2022.100009] [Cited by in Crossref: 6] [Cited by in F6Publishing: 10] [Article Influence: 6.0] [Reference Citation Analysis]
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Chen K, Chen Z, Yang S, Wu S, Zhang Y, Shi F. Organocatalytic Atroposelective Synthesis of N−N Axially Chiral Indoles and Pyrroles by De Novo Ring Formation. Angewandte Chemie 2022;134. [DOI: 10.1002/ange.202116829] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
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Yang H, Sun HR, He RQ, Yu L, Hu W, Chen J, Yang S, Zhang GG, Zhou L. Organocatalytic cycloaddition of alkynylindoles with azonaphthalenes for atroposelective construction of indole-based biaryls. Nat Commun 2022;13:632. [PMID: 35110529 DOI: 10.1038/s41467-022-28211-0] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 12.0] [Reference Citation Analysis]
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Wu P, Yu L, Gao C, Cheng Q, Deng S, Jiao Y, Tan W, Shi F. Design and Synthesis of Axially Chiral Aryl-Pyrroloindoles via the Strategy of Organocatalytic Asymmetric (2 + 3) Cyclization. Fundamental Research 2022. [DOI: 10.1016/j.fmre.2022.01.002] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 7.0] [Reference Citation Analysis]
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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]
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