5335-87-5Relevant articles and documents
Rearrangement of alkynyl sulfoxides catalyzed by gold(I) complexes
Shapiro, Nathan D.,Toste, F. Dean
, p. 4160 - 4161 (2007)
A series of gold(I)-catalyzed rearrangement reactions of alkynyl sulfoxides are reported. Homopropargylsulfoxides are rearranged to benzothiepinones or benzothiopines, while α-thioenones are formed in the reaction of propargylsulfoxides. The proposed mech
Application of Bulky NHC-Rhodium Complexes in Efficient S-Si and S-S Bond Forming Reactions
Bo?t, Ma?gorzata,?ak, Patrycja
supporting information, p. 17579 - 17585 (2021/11/18)
The efficient and straightforward syntheses of silylthioethers and disulfides are presented. The synthetic methodologies are based on new rhodium complexes containing bulky N-heterocyclic carbene (NHC) ligands that turned out to be efficient catalysts in thiol and thiol-silane coupling reactions. These green protocols, which use easily accessible reagents, allow obtaining compounds containing S-Si and S-S bonds in solvent-free conditions. Additionally, preliminary tests on coupling of mono- and octahydro-substituted spherosilicates with selected thiols have proved to be very promising and showed that these catalytic systems can be used for the synthesis of a novel class of functionalized silsesquioxane derivatives.
Cobalt catalysed aminocarbonylation of thiols in batch and flow for the preparation of amides
Domínguez, Gema,Ordu?a, Jose Maria,Pérez-Castells, Javier
, p. 30398 - 30406 (2021/10/20)
The synthesis of amides from thiols through a cobalt-catalyzed aminocarbonylation is shown. After optimizing all the reaction parameters, the methodology makes possible the obtention of amides with variable yields, while competing reactions such as the formation of disulfides and ureas can be limited. The process works well with aromatic thiols with electron donating groups (EDG) whereas other thiols give reaction with lower yields. The previous process has been transferred and optimized into flow equipment, thus allowing using less CO in a safer way, and permitting the scaling up of the synthesis. Two drugs, moclobemide and itopride were prepared with this methodology, albeit only in the second case with good results. A mechanistic pathway is proposed.
