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For: 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]
Number Citing Articles
1 Zhao W, Li BJ. Directing Group Repositioning Strategy Enabled Site- and Enantioselective Addition of Heteroaromatic C-H Bonds to Acyclic Internal Alkenes. J Am Chem Soc 2023. [PMID: 36917558 DOI: 10.1021/jacs.3c00095] [Reference Citation Analysis]
2 Mondal S, Bera R, Chowdhury D, Dana S, Baidya M. Redox-Neutral Ruthenium(II)-Catalyzed Enol-Directed Arene C-H Alkylation with Maleimides. Org Lett 2023;25:70-5. [PMID: 36579895 DOI: 10.1021/acs.orglett.2c03858] [Reference Citation Analysis]
3 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]
4 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]
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6 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]
7 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]
8 Xiao X, Chen B, Yao YP, Zhou HJ, Wang X, Wang NZ, Chen FE. Construction of Non-Biaryl Atropisomeric Amide Scaffolds Bearing a C-N Axis via Enantioselective Catalysis. Molecules 2022;27:6583. [PMID: 36235120 DOI: 10.3390/molecules27196583] [Reference Citation Analysis]
9 Sun X, Lin EZ, Li BJ. Iridium-Catalyzed Branch-Selective and Enantioselective Hydroalkenylation of α-Olefins through C-H Cleavage of Enamides. J Am Chem Soc 2022. [PMID: 36121772 DOI: 10.1021/jacs.2c07477] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
10 Mandal D, Roychowdhury S, Biswas JP, Maiti S, Maiti D. Transition-metal-catalyzed C-H bond alkylation using olefins: recent advances and mechanistic aspects. Chem Soc Rev 2022;51:7358-426. [PMID: 35912472 DOI: 10.1039/d1cs00923k] [Reference Citation Analysis]
11 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]
12 Wang ZH, Liu JH, Zhang YP, Zhao JQ, You Y, Zhou MQ, Han WY, Yuan WC. Cu-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of N-2,2,2-Trifluoroethylisatin Ketimines Enables the Desymmetrization of N-Arylmaleimides: Access to Enantioenriched F3C-Containing Octahydropyrrolo[3,4-c]pyrroles. Org Lett 2022. [PMID: 35622347 DOI: 10.1021/acs.orglett.2c01510] [Cited by in Crossref: 3] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
13 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]
14 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]
15 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]
16 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]
17 Yin C, Li L, Yu C. Rh(III)-catalyzed C-H annulation of sulfoxonium ylides with iodonium ylides towards isocoumarins. Org Biomol Chem 2022;20:1112-6. [PMID: 35040469 DOI: 10.1039/d1ob02273c] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 6.0] [Reference Citation Analysis]
18 Gurupadaswamy HD, Ranganatha VL, Ramu R, Patil SM, Khanum SA. Competent synthesis of biaryl analogs via asymmetric Suzuki–Miyaura cross-coupling for the development of anti-inflammatory and analgesic agents. J IRAN CHEM SOC 2022;19:2421-36. [DOI: 10.1007/s13738-021-02460-0] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 8.0] [Reference Citation Analysis]
19 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]
20 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]
21 Liu S, Shi Y, Xue C, Zhang L, Zhou L, Song M. Maleimides in Directing‐Group‐Controlled Transition‐Metal‐Catalyzed Selective C−H Alkylation. Eur J Org Chem 2021;2021:5862-79. [DOI: 10.1002/ejoc.202101262] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
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. 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]
23 Reddy Singam MK, Suri Babu U, Suresh V, Nanubolu JB, Sridhar Reddy M. Rhodium-Catalyzed Annulation of Phenacyl Ammonium Salts with Propargylic Alcohols via a Sequential Dual C-H and a C-C Bond Activation: Modular Entry to Diverse Isochromenones. Org Lett 2021;23:7888-93. [PMID: 34612648 DOI: 10.1021/acs.orglett.1c02890] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
24 Chen L, Chen J, Zhang Y, He X, Han Y, Xiao Y, Lv G, Lu X, Teng F, Sun Q, Li J. Atroposelective carbonylation of aryl iodides with amides: facile synthesis of enantioenriched cyclic and acyclic amides. Org Chem Front 2021;8:6067-73. [DOI: 10.1039/d1qo01147b] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]