| Literature DB >> 31216118 |
Farid Ouhib1, Bruno Grignard1, Elias Van Den Broeck2, André Luxen3, Koen Robeyns4, Veronique Van Speybroeck2, Christine Jerome1, Christophe Detrembleur1.
Abstract
α-Alkylidene cyclic carbonates (αCCs) recently emerged as attractive CO2 -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 CO2 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.Entities:
Keywords: carbon dioxide; domino process; organocatalysis; polymerization; synthetic methods
Year: 2019 PMID: 31216118 DOI: 10.1002/anie.201905969
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336