Bifunctional Monothiosquaramide-Catalyzed Enantioselective Addition of Masked Acyl Cyanide to Isatins: Umpolung Strategy for the Total Synthesis of (<i>S</i>)-(-)-Dioxibrassinin and (<i>R</i>)-(+)-Spirobrassinin. [PDF]
Reis FAA +7 more
europepmc +1 more source
Recent developments in the organocatalytic asymmetric cycloaddition/annulation reactions involving indolylmethanols. [PDF]
Patel A, Harshit, Iype E, Kumar I.
europepmc +1 more source
Asymmetric Mannich reaction of aromatic imines with malonates in the presence of multifunctional catalysts. [PDF]
Kriis K +5 more
europepmc +1 more source
Catalytic Asymmetric Hydration of Alkenes. [PDF]
Hatano H +13 more
europepmc +1 more source
Heterogeneous organocatalysis: the proline case. [PDF]
de Carvalho GSG +3 more
europepmc +1 more source
A Multicatalytic Cascade for the Stereoselective Synthesis of 1,4-Chiral Nitro Alcohols. [PDF]
Ascaso-Alegre C +4 more
europepmc +1 more source
Performance-enhancing asymmetric catalysis unlocks tuning without rebuilding. [PDF]
Deng Z, Johnston JN.
europepmc +1 more source
Role of 2-Hydroxyimines in Chiral Phosphoric Acid-Catalyzed Mannich-Type Reactions: Enhancing Reactivity and Selectivity via Dimerization. [PDF]
Hecht M +8 more
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Asymmetric Organocatalysis: From Infancy to Adolescence
AbstractAfter an initial period of validating asymmetric organocatalysis by using a wide range of important model reactions that constitute the essential tools of organic synthesis, the time has now been reached when organocatalysis can be used to address specific issues and solve pending problems of stereochemical relevance.
Alessandro Massi, Alessandro Dondoni
exaly +5 more sources
Cinchona Alkaloids in Asymmetric Organocatalysis [PDF]
This article reviews the applications of cinchona alkaloids as asymmetric catalysts. In the last few years, characterized by the resurgence of interest in asymmetric organocatalysis, cinchona derivatives have been shown to catalyze an outstanding array of chemical reactions, often with remarkable stereoselectivity. This work presents an overview of the
Marcelli, T., Hiemstra, H.
exaly +4 more sources

