Angewandte Chemie International Edition · 2019 · 39 citations · 35 references
Natural SciencesChemical EngineeringChemistryOrganic ChemistryPolymer ChemistryReaction EngineeringDiversity-oriented SynthesisOrganic SynthesisCatalytic SynthesisChemoselective CatalysisChemoselective FunctionalizationChemoselective SynthesisCyclic Carbonate SynthesisFormation Of Complex Organic MoleculesRenewable Feedstock DesignSubstrate Scope
Abstract α‐Alkylidene cyclic carbonates (αCCs) recently emerged as attractive CO 2 ‐sourced synthons for the construction of complex organic molecules. Herein, we report the transformation of αCCs into novel families of sulfur‐containing compounds by organocatalyzed chemoselective addition of thiols, following a domino process that is switched on/off depending on the desired product. The process is extremely fast and versatile in substrate scope, provides selectively linear thiocarbonates or elusive tetrasubstituted ethylene carbonates with high yields following a 100 % atom economy reaction, and valorizes CO 2 as a renewable feedstock. It is also exploited to produce a large diversity of unprecedented functional polymers. It constitutes a robust platform for the design of new sulfur‐containing organic synthons and important families of polymers.
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