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| For: | Stone EA, Cutrona KJ, Miller SJ. Asymmetric Catalysis upon Helically Chiral Loratadine Analogues Unveils Enantiomer-Dependent Antihistamine Activity. J Am Chem Soc 2020;142:12690-8. [PMID: 32579347 DOI: 10.1021/jacs.0c03904] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis] |
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| Number | Citing Articles |
| 1 | Tang Y, Miller SJ. Catalytic Enantioselective Synthesis of Pyridyl Sulfoximines. J Am Chem Soc 2021;143:9230-5. [PMID: 34124892 DOI: 10.1021/jacs.1c04431] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis] |
| 2 | Schmidt TA, Sparr C. Catalyst-Controlled Stereoselective Barton-Kellogg Olefination. Angew Chem Int Ed Engl 2021;60:23911-6. [PMID: 34416071 DOI: 10.1002/anie.202109519] [Reference Citation Analysis] |
| 3 | Huang S, Wen H, Tian Y, Wang P, Qin W, Yan H. Organocatalytic Enantioselective Construction of Chiral Azepine Skeleton Bearing Multiple-Stereogenic Elements. Angew Chem Int Ed Engl 2021. [PMID: 34235834 DOI: 10.1002/anie.202108040] [Cited by in F6Publishing: 1] [Reference Citation Analysis] |
| 4 | Wang L, Shi F, Qi C, Xu W, Xiong W, Kang B, Jiang H. Stereodivergent synthesis of β-iodoenol carbamates with CO2 via photocatalysis. Chem Sci 2021;12:11821-30. [PMID: 34659721 DOI: 10.1039/d1sc03366b] [Reference Citation Analysis] |
| 5 | Chan YC, Sak MH, Frank SA, Miller SJ. Tunable and Cooperative Catalysis for Enantioselective Pictet-Spengler Reaction with Varied Nitrogen-Containing Heterocyclic Carboxaldehydes. Angew Chem Int Ed Engl 2021;60:24573-81. [PMID: 34487418 DOI: 10.1002/anie.202109694] [Reference Citation Analysis] |