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For: 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]
Number Citing Articles
1 Bao H, Chen Y, Yang X. Catalytic Asymmetric Synthesis of Axially Chiral Diaryl Ethers through Enantioselective Desymmetrization. Angew Chem Int Ed Engl 2023;62:e202300481. [PMID: 36760025 DOI: 10.1002/anie.202300481] [Reference Citation Analysis]
2 Wang LY, Miao J, Zhao Y, Yang BM. Chiral Acid-Catalyzed Atroposelective Indolization Enables Access to 1,1'-Indole-Pyrroles and Bisindoles Bearing a Chiral N-N Axis. Org Lett 2023;25:1553-7. [PMID: 36857743 DOI: 10.1021/acs.orglett.3c00237] [Reference Citation Analysis]
3 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]
4 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]
5 Choi S, Guo MC, Coombs GM, Miller SJ. Catalytic Asymmetric Synthesis of Atropisomeric N-Aryl 1,2,4-Triazoles. J Org Chem 2023. [PMID: 36705994 DOI: 10.1021/acs.joc.2c02727] [Reference Citation Analysis]
6 Portolani C, Centonze G, Righi P, Bencivenni G. Role of Cinchona Alkaloids in the Enantio- and Diastereoselective Synthesis of Axially Chiral Compounds. Acc Chem Res 2022;55:3551-71. [PMID: 36475607 DOI: 10.1021/acs.accounts.2c00515] [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 Xu J, Grosslight S, Mack KA, Nguyen SC, Clagg K, Lim N, Timmerman JC, Shen J, White NA, Sirois LE, Han C, Zhang H, Sigman MS, Gosselin F. Atroposelective Negishi Coupling Optimization Guided by Multivariate Linear Regression Analysis: Asymmetric Synthesis of KRAS G12C Covalent Inhibitor GDC-6036. J Am Chem Soc 2022. [DOI: 10.1021/jacs.2c09917] [Reference Citation Analysis]
9 Portolani C, Centonze G, Luciani S, Pellegrini A, Righi P, Mazzanti A, Ciogli A, Sorato A, Bencivenni G. Synthesis of Atropisomeric Hydrazides by One-Pot Sequential Enantio- and Diastereoselective Catalysis. Angew Chem Int Ed Engl 2022;61:e202209895. [PMID: 36036383 DOI: 10.1002/anie.202209895] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
10 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]
11 Han T, Zhang Z, Wang M, Xu L, Mei G. The Rational Design and Atroposelective Synthesis of Axially Chiral C2‐Arylpyrrole‐Derived Amino Alcohols. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202207517] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
12 Xu Q, Zhang H, Ge FB, Wang XM, Zhang P, Lu CJ, Liu RR. Cu(I)-Catalyzed Asymmetric Arylation of Pyrroles with Diaryliodonium Salts toward the Synthesis of N-N Atropisomers. Org Lett 2022. [PMID: 35452582 DOI: 10.1021/acs.orglett.2c00812] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
13 Liang D, Chen JR, Tan LP, He ZW, Xiao WJ. Catalytic Asymmetric Construction of Axially and Centrally Chiral Heterobiaryls by Minisci Reaction. J Am Chem Soc 2022. [PMID: 35322666 DOI: 10.1021/jacs.2c01116] [Cited by in Crossref: 8] [Cited by in F6Publishing: 11] [Article Influence: 8.0] [Reference Citation Analysis]