Amanote Research
Register
Sign In
Switching Diastereoselectivity in Catalytic Enantioselective (3+2) Cycloadditions of Azomethine Ylides Promoted by Metal Salts and Privileged Segphos-Derived Ligands
doi 10.1021/acs.joc.9b00267.s002
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Switching Diastereoselectivity in Catalytic Enantioselective (3+2) Cycloadditions of Azomethine Ylides Promoted by Metal Salts and Privileged Segphos-Derived Ligands
Enantioselective Dearomative [3 + 2] Cycloadditions of Indoles With Azomethine Ylides Derived From Alanine Imino Esters
Organic Chemistry Frontiers
Organic Chemistry
Reactivity of 1,2-Diaza-1,3-Dienes With Azomethine Ylides: [3+4] Versus [3+2] Cycloadditions
European Journal of Organic Chemistry
Organic Chemistry
Theoretical Chemistry
Physical
Asymmetric Catalysis Special Feature Part I: Catalytic Enantioselective Intermolecular Cycloadditions of 2-Diazo-3,6-Diketoester-Derived Carbonyl Ylides With Alkene Dipolarophiles
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
[3 + 2]-Cycloadditions of Azomethine Imines and Ynolates
Frontispiece: Catalytic Enantioselective and Regioselective [3+3] Cycloadditions Using 2-Indolylmethanols as 3 C Building Blocks
Chemistry - A European Journal
Organic Chemistry
Catalysis
Chemistry
Multicomponent Diastereoselective Synthesis of Indolizidines via 1,3-Dipolar Cycloadditions of Azomethine Ylides
Synthesis
Organic Chemistry
Catalysis
Silver-Catalysed Multicomponent 1,3-Dipolar Cycloaddition of 2-Oxoaldehydes-Derived Azomethine Ylides
Tetrahedron
Organic Chemistry
Biochemistry
Drug Discovery
CuICatalyzed Asymmetric [3 + 2] Cycloaddition of Azomethine Ylides With Cyclobutenones