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Cited by in F6Publishing
For: Rozsar D, Formica M, Yamazaki K, Hamlin TA, Dixon DJ. Bifunctional Iminophosphorane-Catalyzed Enantioselective Sulfa-Michael Addition to Unactivated α,β-Unsaturated Amides. J Am Chem Soc 2022;144:1006-15. [PMID: 34990142 DOI: 10.1021/jacs.1c11898] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Nieuwland C, Fonseca Guerra C. How the Chalcogen Atom Size Dictates the Hydrogen‐Bond Donor Capability of Carboxamides, Thioamides, and Selenoamides. Chemistry A European J 2022;28. [DOI: 10.1002/chem.202200755] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
2 Bai YJ, Cheng ML, Zheng XH, Zhang SY, Wang PA. Chiral Cyclopropenimine-catalyzed Asymmetric Michael Addition of Bulky Glycine Imine to α,β-Unsaturated Isoxazoles. Chem Asian J 2022;:e202200131. [PMID: 35415949 DOI: 10.1002/asia.202200131] [Reference Citation Analysis]
3 . Iminophosphorane Catalyst Permits Enantioselective Sulfa-Michael Addition to α,β-Unsaturated Amides. Synfacts 2022;18:0425. [DOI: 10.1055/s-0041-1737389] [Reference Citation Analysis]