Publication | Closed Access
Efficient Synthesis of α‐Ketothioamides From α‐Nitroketones, Amines or DMF and Elemental Sulfur Under Oxidant‐Free Conditions
22
Citations
36
References
2021
Year
Chemical EngineeringGeneral ProtocolEngineeringAliphatic α‐KetothioamidesNovel OrganocatalystsNatural SciencesDiversity-oriented SynthesisOrganic ChemistryCatalysisElemental SulfurChemistryEfficient SynthesisSynthesis MethodSynthetic ChemistryEnantioselective SynthesisAvailable α‐NitroketonesOxidant‐free Conditions
Abstract We have developed a practical, general protocol for denitration of readily available α‐nitroketones with sulfur and amines to access a broad range of α‐ketothioamides under mild conditions. Such a reaction proceeds under metal‐, oxidant‐, and catalyst‐free conditions to provide synthetically useful α‐ketothioamides. Furthermore, the mild reaction conditions tolerate a wide range of substrates especially for the synthesis of aliphatic α‐ketothioamides which are rarely reported.
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