177336-50-4Relevant academic research and scientific papers
Highly enantioselective organocatalytic sulfa-michael addition to α, β-unsaturated ketones
Rana, Nirmal K.,Selvakumar, Sermadurai,Singh, Vinod K.
supporting information; experimental part, p. 2089 - 2091 (2010/06/16)
"Chemical Equation Presented" A cinchona alkaloid-derived urea was found to be an efficient organocatalyst for catalyzing enantioselective conjugate addition between thiols and various α,β-unsaturated ketones to provide optically active sulfides with high
Asymmetrie ruthenium-catalyzed 1,4-additions of aryl thiols to enones
Badoiu, Andrei,Bernardinelli, Gerald,Besnard, Celine,Peter Kuendig
supporting information; experimental part, p. 193 - 200 (2010/04/25)
Well defined, stable, one-point binding ruthenium complexes 1 and 2 selectively bind and activate α,β-unsaturated carbonyl compounds for cycloaddition reactions. These mild Lewis acids catalyze asymmetric 1,4-addition reactions of aryl thiols to enones wi
