DABSO – A Reagent to Revolutionize Organosulfur Chemistry
Michael C. Willis, Jonathan A. Andrews
Abstract
Abstract The introduction of easy-to-handle SO2 surrogates has transformed the field of sulfur chemistry, enabling methodologies utilizing SO2 to be carried out without specialized apparatus, and paving the way for the development of new procedures. This review highlights some of the varied and significant developments associated with one of the most prominent SO2 surrogates: DABSO. 1 Introduction 2 DABSO 3 Reactions with Nucleophilic Reagents 4 Metal-Catalyzed Reactions 4.1 Palladium-Catalyzed Reactions 4.2 Other Transition-Metal Catalysis 5 Radical Reactions 5.1 Aryldiazonium Salts 5.2 Other Aryl Radical Precursors 5.3 Alkyl Radical Precursors 6 Conclusion
Topics & Concepts
ChemistryOrganosulfur compoundsReagentNucleophileArylCatalysisOrganic chemistrySulfurAlkylPalladiumCombinatorial chemistrySulfur-Based Synthesis TechniquesRadical Photochemical ReactionsChemical Synthesis and Reactions