biostudies-literatureZhong ZRoyal Society16115-16126https://www.ebi.ac.uk/biostudies/studies/S-EPMC9724092biostudies-literatureUnknown87(23)Sulfoximines provide aza-analogues of sulfones, with potentially improved properties for medicinal chemistry. The sulfoximine nitrogen also provides an additional vector for the inclusion of other functionality. Here, we report improved conditions for rhodium catalyzed synthesis of sulfoximine (and sulfilimine) carbamates, especially for previously low-yielding carbamates containing π-functionality. Notably we report the preparation of propargyl sulfoximine carbamates to provide an alkyne as a potential click handle. Using Rh₂(esp)₂ as catalyst and a DOE optimization approach provided considerably increased yields.The Journal of organic chemistrySynthesis of Sulfoximine Propargyl Carbamates under Improved Conditions for Rhodium Catalyzed Carbamate Transfer to Sulfoxides.PMC9724092URF\R\201019UF140161Bull JAChesti JZhong ZArmstrong AfalseSynthesis of Sulfoximine Propargyl Carbamates under Improved Conditions for Rhodium Catalyzed Carbamate Transfer to Sulfoxides.Sulfoximines provide aza-analogues of sulfones, with potentially improved properties for medicinal chemistry. The sulfoximine nitrogen also provides an additional vector for the inclusion of other functionality. Here, we report improved conditions for rhodium catalyzed synthesis of sulfoximine (and sulfilimine) carbamates, especially for previously low-yielding carbamates containing π-functionality. Notably we report the preparation of propargyl sulfoximine carbamates to provide an alkyne as a potential click handle. Using Rh₂(esp)₂ as catalyst and a DOE optimization approach provided considerably increased yields.2022-01-01T00:00:00Z2022 Dec2025-04-26T02:16:13.686Z2025-04-06T10:22:55.012ZS-EPMC97240923637900810.1021/acs.joc.2c02083