916830-75-6Relevant academic research and scientific papers
Solvent free enantioselective catalysis with chiral cobalt(iii) Werner complexes via ball milling
Gladysz, John A.,Jameson, Bailey L.,Kabes, Connor Q.
supporting information, p. 17101 - 17107 (2021/10/05)
Enantioselective additions of malonate esters to nitroalkenes can be catalyzed by a variety of salts of chiral cobalt(iii) trications [Co(1,2-diamine)3]3+ in the presence of nitrogen donor bases in acetone. Catalysts that feature enantiopure 1,2-diphenyle
In situ preparation of a multifunctional chiral hybrid organic-inorganic catalyst for asymmetric multicomponent reactions
Garcia-Garcia, Pilar,Zagdoun, Alexandre,Coperet, Christophe,Lesage, Anne,Diaz, Urbano,Corma, Avelino
, p. 2006 - 2012 (2013/05/09)
A chiral mesoporous organosilica material incorporating a urea based-cinchona derivative and propylamine groups was prepared by a co-condensation method. The multisite solid catalyst efficiently promoted the asymmetric multicomponent reaction of aldehydes, malonates and nitromethane.
METHOD FOR PRODUCING PYRROLIDINE COMPOUND
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Page/Page column 95, (2009/10/01)
Provided is a method capable of efficiently producing a compound having a superior HSD1 inhibitory action and a compound useful as a synthetic intermediate therefor, with superior achievability of asymmetric synthesis (i.e., superior selectivity), superior yield, superior safety and superior industrial workability at a low cost. A method of producing a compound represented by the following formula [8]: or a salt thereof, or a solvate thereof, from a compound represented by the following formula [2]: or a reactive derivative thereof, or a salt thereof, or a solvate thereof.
Heterocyclic compounds
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Page/Page column 71, (2010/11/26)
The present invention provides a compound represented by the following formula [1′] or a salt thereof: wherein ring A, R2, R3, R4 and X are as defined in the description, and an agent for the treatment or prophylaxis of a
