Amanote Research
Register
Sign In
Enantioselective Organocatalytic Tandem Michael-Aldol Reactions: One-Pot Synthesis of Chiral Thiochromenes
doi 10.1021/ja063328m.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Enantioselective Organocatalytic Tandem Michael-Aldol Reactions: One-Pot Synthesis of Chiral Thiochromenes
One-Pot Organocatalytic Domino Michael-Aldol and Intramolecular SN2 Reactions. Asymmetric Synthesis of Highly Functionalized Epoxycyclohexanone Derivatives
Enantioselective Organocatalytic Double Michael Addition Reactions
Synthesis of 2,3,4-Trisubstituted Thiochromanes Using an Organocatalytic Enantioselective Tandem Michael-Henry Reaction
Advanced Synthesis and Catalysis
Organic Chemistry
Catalysis
Asymmetric Synthesis of Highly Functionalized Tetrahydropyrans via a One-Pot Organocatalytic Michael/Henry/Ketalization Sequence
Organic Letters
Biochemistry
Organic Chemistry
Theoretical Chemistry
Physical
Tandem Grinding Reactions Involving Aldol Condensation and Michael Addition in Sequence for Synthesis of 3,4,5-Trisubstituted Isoxazoles
RSC Advances
Chemistry
Chemical Engineering
Enantioselective Synthesis of 3-Substituted Isoindolinones via Chiral Phase-Transfer Catalyzed Intramolecular Aza-Michael Reactions
Catalytic Enantioselective Synthesis of Chiral Isatin Derivatives by an Aldol Approach
Synlett
Organic Chemistry
Enantioselective Synthesis of Yohimbine Analogues by an Organocatalytic and Pot-Economic Strategy
