Results 121 to 130 of about 2,722 (150)
Some of the next articles are maybe not open access.

Kinetic Resolution of Secondary Alcohols Catalyzed by Chiral Phosphoric Acids

Angewandte Chemie, 2013
A new electronically tuned binaphthyl-based phosphoric acid is developed, that, in contrast to conventional methods, allows the kinetic resolution of a broad range of secondary alcohols without the need of stoichiometric amounts of base.
Shingo, Harada   +4 more
openaire   +2 more sources

Chiral Phosphoric Acid‐Catalyzed Atroposelective Synthesis of Axially Chiral Aminophosphines

Chinese Journal of Chemistry
Comprehensive SummaryP,N‐Atropisomers are valuable structural motifs, widely utilized as chiral ligands and in various catalytic systems. However, the asymmetric synthesis of these compounds from readily available starting materials remains a significant challenge.
Zi‐Han Wang   +5 more
openaire   +1 more source

Phosphoric Acid-Catalyzed Enantioselective Synthesis of Axially Chiral Cyclobutanamides

Organic Letters
Chiral cyclobutanamide is a privileged scaffold in drug discovery. Here, we describe, for the first time, the synthesis of axially chiral cyclobutanamides via phosphoric acid-catalyzed enantioselective condensation between N-arylcarbamyl cyclobutanones and hydroxylamines.
Guang Cheng   +6 more
openaire   +2 more sources

Controlling Stereoselectivity with Noncovalent Interactions in Chiral Phosphoric Acid Organocatalysis

Chemical Reviews
Chiral phosphoric acids (CPAs) have emerged as highly effective Brønsted acid catalysts in an expanding range of asymmetric transformations, often through novel multifunctional substrate activation modes. Versatile and broadly appealing, these catalysts benefit from modular and tunable structures, and compatibility with additives.
Isaiah O. Betinol   +3 more
openaire   +2 more sources

Aporphinol-Derived Chiral Phosphoric Acids: Synthesis and Catalytic Performance

Organic Letters
A novel series of chiral phosphoric acid (CPA) catalysts based on a bioinspired aporphinol scaffold has been developed. The efficacy of these CPAs is demonstrated through enantioselective transfer hydrogenation of C2-substituted quinolines, achieving excellent enantioselectivities (93-99% enantiomeric excess).
Jun Zhao   +8 more
openaire   +2 more sources

Nitrosobenzene‐Enabled Chiral Phosphoric Acid Catalyzed Enantioselective Construction of Atropisomeric N‐Arylbenzimidazoles

Angewandte Chemie - International Edition, 2021
Wang Xia   +2 more
exaly  

Home - About - Disclaimer - Privacy