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For: 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: 19.5] [Reference Citation Analysis]
Number Citing Articles
1 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]
2 Kong L, Zou Y, Li XX, Zhang XP, Li X. Rhodium-catalyzed enantioselective C-H alkynylation of sulfoxides in diverse patterns: desymmetrization, kinetic resolution, and parallel kinetic resolution. Chem Sci 2023;14:317-22. [PMID: 36687346 DOI: 10.1039/d2sc05310a] [Reference Citation Analysis]
3 Zhang X, Liu YZ, Shao H, Ma X. Advances in Atroposelectively De Novo Synthesis of Axially Chiral Heterobiaryl Scaffolds. Molecules 2022;27. [PMID: 36500610 DOI: 10.3390/molecules27238517] [Reference Citation Analysis]
4 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]
5 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]
6 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]
7 Niu C, Zhou Y, Chen Q, Zhu Y, Tang S, Yu ZX, Sun J. Atroposelective Synthesis of N-Arylindoles via Enantioselective N-H Bond Insertion. Org Lett 2022. [PMID: 36190794 DOI: 10.1021/acs.orglett.2c03003] [Reference Citation Analysis]
8 Zhang J, Fan J, Wu Y, Guo Z, Wu J, Xie M. Pd-Catalyzed Atroposelective C–H Acyloxylation Enabling Access to an Axially Chiral Biaryl Phenol Organocatalyst. Org Lett . [DOI: 10.1021/acs.orglett.2c01981] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
9 Liu J, Li Q, Shao Y, Sun J. Atroposelective Synthesis of Axially Chiral C2-Arylindoles via Rhodium-Catalyzed Asymmetric C-H Bond Insertion. Org Lett 2022;24:4670-4. [PMID: 35730740 DOI: 10.1021/acs.orglett.2c01818] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
10 Sarkar S, Samanta R. Weakly Coordinating tert-Amide-Assisted Ru(II)-Catalyzed Synthesis of Azacoumestans via Migratory Insertion of Quinoid Carbene: Application in the Total Synthesis of Isolamellarins. Org Lett 2022;24:4536-41. [PMID: 35735263 DOI: 10.1021/acs.orglett.2c01556] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
11 Yan X, Jiang J, Wang J. A Class of Readily Tunable Planar-Chiral Cyclopentadienyl Rhodium(III) Catalysts for Asymmetric C-H Activation. Angew Chem Int Ed Engl 2022;61:e202201522. [PMID: 35302699 DOI: 10.1002/anie.202201522] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
12 Yu C, Xu Y, Zhang X, Fan X. Synthesis of N-Arylindoles from 2-Alkenylanilines and Diazonaphthalen-2(1H)-ones through Simultaneous Indole Construction and Aryl Introduction. J Org Chem 2022;87:7392-404. [PMID: 35594494 DOI: 10.1021/acs.joc.2c00628] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
13 Liu S, Zhang D, Li C, Li D, Zhou Z. Theoretical Study of Rhodium-Catalyzed Dual C–H Activation to Synthesize C–N Axially Chiral N -Aryloxindoles: Origin of Axial Chirality. Organometallics. [DOI: 10.1021/acs.organomet.1c00687] [Reference Citation Analysis]
14 Yin S, Pan C, Zhang W, Liu C, Zhao F, Gu Q, You S. SCpRh(III)-Catalyzed Enantioselective Synthesis of Atropisomers by C2-Arylation of Indoles with 1-Diazonaphthoquinones. Org Lett . [DOI: 10.1021/acs.orglett.2c01141] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
15 Lahtigui O, Forster D, Duchemin C, Cramer N. Enantioselective Access to 3-Azabicyclo[3.1.0]hexanes by Cp x Rh III Catalyzed C–H Activation and Cp*Ir III Transfer Hydrogenation. ACS Catal . [DOI: 10.1021/acscatal.2c01827] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
16 Zou Y, Wang P, Kong L, Li X. Rhodium-Catalyzed Atroposelective C-H Arylation of (Hetero)Arenes Using Carbene Precursors as Arylating Reagents. Org Lett 2022. [PMID: 35468294 DOI: 10.1021/acs.orglett.2c00968] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
17 Wang P, Cen S, Gao J, Shen A, Zhang Z. Novel Axially Chiral Ligand-Enabled Copper-Catalyzed Asymmetric Oxidative Coupling of 2-Naphthols for the Synthesis of 6,6′-Disubstituted BINOLs. Org Lett . [DOI: 10.1021/acs.orglett.2c00479] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
18 Liao G, Zhang T, Jin L, Wang BJ, Xu CK, Lan Y, Zhao Y, Shi BF. Experimental and Computational Studies on the Directing Ability of Chalcogenoethers in Palladium-Catalyzed Atroposelective C-H Olefination and Allylation. Angew Chem Int Ed Engl 2022;61:e202115221. [PMID: 34985788 DOI: 10.1002/anie.202115221] [Cited by in Crossref: 7] [Cited by in F6Publishing: 9] [Article Influence: 7.0] [Reference Citation Analysis]
19 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]
20 Biswas A, Pan S, Samanta R. Cu(II)-Catalyzed Construction of Heterobiaryls using 1-Diazonaphthoquinones: A General Strategy for the Synthesis of QUINOX and Related P,N Ligands. Org Lett . [DOI: 10.1021/acs.orglett.2c00127] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
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22 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]
23 Shen C, Zhu Y, Shen W, Jin S, Zhong L, Luo S, Xu L, Zhong G, Zhang J. Construction of axial chirality by asymmetric alpha C–H alkenylation of aryl alkenes. Org Chem Front . [DOI: 10.1039/d2qo00803c] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
24 Rao J, Ren X, Zhu X, Guo Z, Wang C, Zhou C. Ruthenium-catalyzed reaction of diazoquinones with arylamines to synthesize diarylamines. Org Chem Front . [DOI: 10.1039/d2qo01134d] [Reference Citation Analysis]
25 Guo S, Zhang Z, Zhu Y, Wei Z, Zhang X, Fan X. Rh(iii)-catalyzed substrate-dependent oxidative (spiro)annulation of isoquinolones with diazonaphthoquinones: selective access to new spirocyclic and oxepine-fused polycyclic compounds. Org Chem Front 2022. [DOI: 10.1039/d2qo01322c] [Reference Citation Analysis]
26 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]
27 Rao J, Zhao J, Zhu X, Guo Z, Wang C, Zhou C. Rhodium-catalyzed reaction of diazoquinones with allylboronates to synthesize allylphenols. Org Chem Front . [DOI: 10.1039/d2qo00626j] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 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]
29 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]
30 Li Z, Chen Y, Wang C, Xu G, Shao Y, Zhang X, Tang S, Sun J. Construction of C−C Axial Chirality via Asymmetric Carbene Insertion into Arene C−H Bonds. Angewandte Chemie 2021;133:25918-25922. [DOI: 10.1002/ange.202110430] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
31 Li Z, Chen Y, Wang C, Xu G, Shao Y, Zhang X, Tang S, Sun J. Construction of C-C Axial Chirality via Asymmetric Carbene Insertion into Arene C-H Bonds. Angew Chem Int Ed Engl 2021;60:25714-8. [PMID: 34597448 DOI: 10.1002/anie.202110430] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
32 Wang J, Li M. Recent Advances on Transition-Metal-Catalyzed Asymmetric C–H Arylation Reactions. Synthesis 2021. [DOI: 10.1055/a-1677-5870] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
33 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]
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36 Liu CX, Zhang WW, Yin SY, Gu Q, You SL. Synthesis of Atropisomers by Transition-Metal-Catalyzed Asymmetric C-H Functionalization Reactions. J Am Chem Soc 2021;143:14025-40. [PMID: 34432467 DOI: 10.1021/jacs.1c07635] [Cited by in Crossref: 51] [Cited by in F6Publishing: 60] [Article Influence: 25.5] [Reference Citation Analysis]
37 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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41 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]
42 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]