Amanote Research
Register
Sign In
Nucleophilic Acylation of O-Quinone Methides: An Umpolung Strategy for the Synthesis of A-Aryl Ketones and Benzofurans
doi 10.1021/ja068189n.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Substituents on Quinone Methides Strongly Modulate Formation and Stability of Their Nucleophilic Adducts
Journal of the American Chemical Society
Biochemistry
Colloid
Catalysis
Chemistry
Surface Chemistry
Alkyl, Unsaturated, (Hetero)aryl, and N-Protected A-Amino Ketones by Acylation of Organometallic Reagents
Alkyl, Unsaturated, (Hetero)aryl, and N-Protected A-Amino Ketones by Acylation of Organometallic Reagents
Dakin-West Synthesis of B-Aryl Ketones
Enantioselective Organocatalytic Activation of Vinylidene-Quinone Methides (VQMs)
Chemical Communications
Surfaces
Alloys
Materials Chemistry
Coatings
Metals
Optical
Magnetic Materials
Films
Catalysis
Chemistry
Electronic
Composites
Ceramics
Palladium-Catalyzed Synthesis of Aryl Ketones by Coupling of Aryl Bromides With an Acyl Anion Equivalent
Umpolung Addition of Aldehydes to Aryl Imines
Angewandte Chemie
Triple Nucleophilic Attack of Nitromethane on (2-Iminoaryl)divinyl Ketones: A Domino Synthetic Strategy for Hexahydrophenanthridinones
Michael Additions of Highly Basic Enolates Toortho-Quinone Methides
Organic Letters
Biochemistry
Organic Chemistry
Theoretical Chemistry
Physical