ol6b02981_si_003.cif (552.53 kB)
Palladium-Catalyzed Stereoselective Formation of Substituted Allylic Thioethers and Sulfones
datasetposted on 2016-11-18, 20:03 authored by José Enrique Gómez, Wusheng Guo, Arjan W. Kleij
A general method is reported for the stereoselective preparation of highly functionalized allylic thioethers. This protocol is based on a Pd-catalyzed thiolation of modular vinyl cyclic carbonate substrates and features high (Z)-selectivity, good yields, minimal waste, ample product scope, and operational simplicity. A one-pot strategy was used for the stereoselective formation of pharma-relevant allylic sulfones derived from their in situ prepared thioether precursors.
vinyl cyclic carbonate substratesselectivitySulfoneSubstituted Allylic Thioethersfunctionalized allylic thioethersstereoselective preparationsimplicitystereoselective formationproduct scopemethodPd-catalyzed thiolationthioether precursorsone-pot strategypharma-relevant allylic sulfonesPalladium-Catalyzed Stereoselective Formationyield