3-(((1S,3S)-3-((R)-Hydroxy(4-(trifluoromethyl)phenyl)methyl)-4-oxocyclohexyl)methyl)pentane-2,4-dione: Design and Synthesis of New Stereopure Multi-Target …
The chiral drug candidates have more effective binding affinities for their specific protein or
receptor site for the onset of pharmacological action. Achieving all carbon stereopure …
receptor site for the onset of pharmacological action. Achieving all carbon stereopure …
A general and mild synthetic method for fused-ring electronic acceptors
Fused-ring electronic acceptors (FREAs) have transformed the field of organic solar cells.
However, the prevailing syntheses of FREAs suffer from low yield, difficulty in separation …
However, the prevailing syntheses of FREAs suffer from low yield, difficulty in separation …
A 2000 to 2020 Practitioner's Guide to Chiral Amine‐Based Enantioselective Aldol Reactions: Ketone Substrates, Best Methods, in Water Reaction Environments, and …
An extensive introduction is provided for the non‐expert regarding enantioselective, amine
catalyzed, aldol reactions (Sections 1–3). There, a broad perspective is provided regarding …
catalyzed, aldol reactions (Sections 1–3). There, a broad perspective is provided regarding …
Enantioselective Catalytic Aldol Reactions in the Presence of Knoevenagel Nucleophiles: A Chemoselective Switch Optimized in Deep Eutectic Solvents Using …
H Al Beiruty, SS Zhylinska, N Kutateladze… - Molecules, 2023 - mdpi.com
In the presence of different nucleophilic Knoevenagel competitors, cyclic and acyclic
ketones have been shown to undergo highly chemoselective aldol reactions with aldehydes …
ketones have been shown to undergo highly chemoselective aldol reactions with aldehydes …