Amanote Research
Register
Sign In
Correction to Phenolic Oxidation Using H2O2 via in Situ Generated Para-Quinone Methides for the Preparation of Para-Spiroepoxydienones
doi 10.1021/acs.orglett.9b03075.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Organocatalytic Asymmetric Formal [4 + 2] Cycloaddition of in Situ Oxidation-Generated Ortho-Quinone Methides and Aldehydes
Frontispiece: Palladium-Catalyzed Enantioselective Addition of Chiral Metal Enolates to in Situ Generated Ortho -Quinone Methides
Angewandte Chemie - International Edition
Catalysis
Chemistry
Frontispiz: Palladium-Catalyzed Enantioselective Addition of Chiral Metal Enolates to in Situ Generated Ortho -Quinone Methides
Angewandte Chemie
Correction: An Organic-Base Catalyzed Asymmetric 1,4-Addition of Tritylthiol to in Situ Generated Aza-O-Quinone Methides at the H2o/DCM Interface
Chemical Communications
Surfaces
Alloys
Materials Chemistry
Coatings
Metals
Optical
Magnetic Materials
Films
Catalysis
Chemistry
Electronic
Composites
Ceramics
Diastereo- And Enantioselective 1,6-Conjugate Addition of 2Azaarylacetamides to Para-Quinone Methides
Metal-Free One-Pot Synthesis of 3-Phosphinoylbenzofurans via Phospha-Michael Addition/Cyclization of H-Phosphine Oxides and in Situ Generated Ortho-Quinone Methides
Organocatalytic Enantioselective Conjugate Addition of 2-Naphthols to Ortho-Hydroxyphenyl Substituted Para-Quinone Methides: Access to Unsymmetrical Triarylmethanes
RSC Advances
Chemistry
Chemical Engineering
Bis(amino)cyclopropenylidene Catalyzed RauhutCurrier Reaction Between ,-Unsaturated Carbonyl Compounds and Para-Quinone Methides
Enantioselective Organocatalytic 1,6-Addition of Azlactones to Para-Quinone Methides: An Access to ,-Disubstituted and ,-Diaryl--Amino Acid Esters