113036-75-2Relevant articles and documents
High-Pressure Asymmetric Michael Additions of Thiols, Nitromethane, and Methyl Oxoindancarboxylate to Enones
Sera, Akira,Takagi, Kazuhiro,Katayama, Hirohito,Yamada, Hiroaki
, p. 1157 - 1161 (1988)
Quinine- and quinidine-catalyzed asymmetric Michael additions of benzenethiols 3 to cyclohexenones 4 (reaction 1, Scheme I), of nitromethane (6) to chalcone (7) (reaction 2), and of methyl oxoindancarboxylate 9 to methyl vinyl ketone (10) (reaction 3) are
Interference of the surface of the solid on the performance of tethered molecular catalysts
Hong, Junghyun,Zaera, Francisco
experimental part, p. 13056 - 13065 (2012/10/08)
The catalytic performance of cinchonidine in the promotion of thiol additions to conjugated ketones was used as a probe to assess the tethering of molecular functionality onto solid surfaces using well-known "click" chemistry involving easy-to-react linke
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
