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<i>N</i>‐Alkylations of <i>N</i>H‐Sulfoximines and <i>N</i>H‐Sulfondiimines with Alkyl Halides Mediated by Potassium Hydroxide in Dimethyl Sulfoxide
82
Citations
40
References
2014
Year
HalogenationDimethyl SulfoxideBioorganic ChemistryPharmaceutical ChemistryActive SuloxifenNatural SciencesN H‐sulfondiiminesChemical DerivativeOrganic ChemistryChemistryPotassium HydroxideAlkyl Halides MediatedPharmacologyInaccessible NSynthetic Chemistry
Abstract A general method for the N ‐alkylation of N H‐sulfoximines and N H‐sulfondiimines has been developed, employing alkyl bromides with KOH in DMSO at room temperature. A variety of previously inaccessible N ‐alkylated sulfoximines and sulfondiimines was prepared in good to excellent yields (up to 97%). As an application, the conditions were used to access the biologically active Suloxifen. magnified image
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