Amanote Research
Register
Sign In
Design of Bronsted Acid-Assisted Chiral Bronsted Acid Catalyst Bearing a Bis(triflyl)methyl Group for a Mannich-Type Reaction
doi 10.1021/ol060939a.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Design of Chiral N-Triflyl Phosphoramide as a Strong Chiral Bronsted Acid and Its Application to Asymmetric Diels-Alder Reaction
Enantioselective Friedel-Crafts Reaction of Electron-Rich Alkenes Catalyzed by Chiral Bronsted Acid
Chiral Bronsted Acid Catalyzed Enantioselective Dehydrative Nazarov-Type Electrocyclization of Aryl and 2Thienyl Vinyl Alcohols
Chiral Bronsted Acid Catalyzed Enantioselective Dehydrative Nazarov-Type Electrocyclization of Aryl and 2Thienyl Vinyl Alcohols
Chiral Bronsted Acid Catalyzed Enantioselective Dehydrative Nazarov-Type Electrocyclization of Aryl and 2Thienyl Vinyl Alcohols
Group-Assisted Purification Chemistry for Asymmetric Mannich-Type Reaction of Chiral N-Phosphonyl Imines With Azlactones Leading to Syntheses of -Quaternary ,-Diamino Acid Derivatives
Surfactant-Type Bronsted Acid Catalyzed Dehydrative Nucleophilic Substitutions of Alcohols in Water
The Structure of the Strongest Bronsted Acid: The Carborane Acid H(CHB11Cl11)
Solvent-Free, Mechanochemically Scalable Synthesis of 2,3-Dihydroquinazolin-4(1h)-One Using Bronsted Acid Catalyst
