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For: 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: 13.5] [Reference Citation Analysis]
Number Citing Articles
1 Wu W, Fan S, Wu X, Fang L, Zhu J. Cobalt Homeostatic Catalysis for Coupling of Enaminones and Oxadiazolones to Quinazolinones. J Org Chem 2023. [PMID: 36705660 DOI: 10.1021/acs.joc.2c01934] [Reference Citation Analysis]
2 Yu L, Liu J, Xiang S, Lu T, Ma P, Zhao Q. Silver-Catalyzed Direct Nucleophilic Cyclization: Enantioselective De Novo Synthesis of C-C Axially Chiral 2-Arylindoles. Org Lett 2023;25:522-7. [PMID: 36652713 DOI: 10.1021/acs.orglett.2c04234] [Reference Citation Analysis]
3 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]
4 Yan Y, Li M, Shi Q, Huang M, Li W, Cao L, Zhang X. Atropoenantioselective Arylation of 5‐Amino‐Isothiazoles with Methyl p ‐Quinone Carboxylate. Asian J Org Chem 2023;12. [DOI: 10.1002/ajoc.202200578] [Reference Citation Analysis]
5 Zhao X, Fan C, He J, Luo Y. Rh-Catalyzed [3+2] Annulation of Cyclic Ketimines and Alkynyl Chloride: A Strategy for Accessing Unsymmetrically Substituted and Highly Functionalizable Indenes. Org Lett 2022;24:9169-73. [PMID: 36503272 DOI: 10.1021/acs.orglett.2c02717] [Reference Citation Analysis]
6 Rodríguez-salamanca P, de Gonzalo G, Carmona JA, López-serrano J, Iglesias-sigüenza J, Fernández R, Lassaletta JM, Hornillos V. Biocatalytic Atroposelective Synthesis of Axially Chiral N-Arylindoles via Dynamic Kinetic Resolution. ACS Catal 2022. [DOI: 10.1021/acscatal.2c06175] [Reference Citation Analysis]
7 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]
8 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]
9 Luo M, Hou Q, Liu S, Zhao Q, Qin R, Peng C, Han B, Zhan G. One-Step Synthesis of Hydropyrrolo[3,2-b]indoles via Cascade Reactions of Oxindole-Derived Nitrones with Allenoates. Org Lett 2022. [DOI: 10.1021/acs.orglett.2c03349] [Reference Citation Analysis]
10 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]
11 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]
12 Mahato S, Sarkar W, Naskar K, Deb I. Rhodium‐Catalyzed CH Functionalization to Construct Annulated Molecules. Handbook of CH‐Functionalization 2022. [DOI: 10.1002/9783527834242.chf0026] [Reference Citation Analysis]
13 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]
14 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]
15 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]
16 Zhang S, Luo ZH, Wang WT, Qian L, Liao JY. Simultaneous Construction of C-N Axial and Central Chirality via Silver-Catalyzed Desymmetrizative [3 + 2] Cycloaddition of Prochiral N-Aryl Maleimides with Activated Isocyanides. Org Lett 2022;24:4645-9. [PMID: 35724978 DOI: 10.1021/acs.orglett.2c01761] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
17 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]
18 Wang ZS, Zhu LJ, Li CT, Liu BY, Hong X, Ye LW. Synthesis of Axially Chiral N-Arylindoles via Atroposelective Cyclization of Ynamides Catalyzed by Chiral Brønsted Acids. Angew Chem Int Ed Engl 2022;61:e202201436. [PMID: 35246909 DOI: 10.1002/anie.202201436] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 7.0] [Reference Citation Analysis]
19 Mei G, Koay WL, Guan C, Lu Y. Atropisomers beyond the C–C axial chirality: Advances in catalytic asymmetric synthesis. Chem 2022. [DOI: 10.1016/j.chempr.2022.04.011] [Cited by in Crossref: 21] [Cited by in F6Publishing: 15] [Article Influence: 21.0] [Reference Citation Analysis]
20 Guo WT, Zhu BH, Chen Y, Yang J, Qian PC, Deng C, Ye LW, Li L. Enantioselective Rh-Catalyzed Azide-Internal-Alkyne Cycloaddition for the Construction of Axially Chiral 1,2,3-Triazoles. J Am Chem Soc 2022. [PMID: 35394289 DOI: 10.1021/jacs.2c01985] [Cited by in Crossref: 3] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
21 Xu S, Huang A, Yang Y, Wang Y, Zhang M, Sun Z, Zhao M, Wei Y, Li G, Hong L. Organocatalytic Enantioselective Construction of Spiroketal Lactones Bearing Axial and Central Chirality via an Asymmetric Domino Reaction. Org Lett 2022. [PMID: 35380447 DOI: 10.1021/acs.orglett.2c00845] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
22 Zhang D, He X, Yang T, Liu S. Insights into the Activation Mode of α-Carbonyl Sulfoxonium Ylides in Rhodium-Catalyzed C-H Activation: A Theoretical Study. ChemistryOpen 2022;:e202100254. [PMID: 35212172 DOI: 10.1002/open.202100254] [Reference Citation Analysis]
23 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]
24 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]
25 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]
26 Wu Y, Liao G, Shi B. Stereoselective construction of atropisomers featuring a C–N chiral axis. Green Synthesis and Catalysis 2022. [DOI: 10.1016/j.gresc.2021.12.005] [Cited by in Crossref: 18] [Cited by in F6Publishing: 25] [Article Influence: 18.0] [Reference Citation Analysis]
27 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]
28 Shao Y, Feng J, Han D, Pan K, Zhang L, Wang Y, Ma Z, Wang P, Yin M, Cheng D. Construction of axially chiral styrene-type allylamines via chiral phosphoric acid-catalyzed asymmetric reductive amination. Org Chem Front 2022;9:764-70. [DOI: 10.1039/d1qo01672e] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [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. 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]
30 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]
31 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]
32 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 2021;133:20587-92. [DOI: 10.1002/ange.202106871] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
33 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]