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Michael reaction

  • Catalytic Direct Asymmetric Michael Reactions

    Catalytic Direct Asymmetric Michael Reactions

  • Recoverable Phospha-Michael Additions Catalyzed by a 4-N,N

    Recoverable Phospha-Michael Additions Catalyzed by a 4-N,N

  • Development of the Interrupted Nazarov Cyclization of Allenyl Vinyl Ketones, with Application to the Total Synthesis of the Cyclooctane Natural Product Roseadione

    Development of the Interrupted Nazarov Cyclization of Allenyl Vinyl Ketones, with Application to the Total Synthesis of the Cyclooctane Natural Product Roseadione

  • Electron Deficient Heterocycle. Examples Abound

    Electron Deficient Heterocycle. Examples Abound

  • Approach and Synthesis of Strychnos Alkaloids

    Approach and Synthesis of Strychnos Alkaloids

  • Advances in the Asymmetric Total Synthesis of Natural Products Using Chiral Secondary Amine Catalyzed Reactions of Α,Β-Unsaturated Aldehydes

    Advances in the Asymmetric Total Synthesis of Natural Products Using Chiral Secondary Amine Catalyzed Reactions of Α,Β-Unsaturated Aldehydes

  • A Novel Aza-Nazarov Cyclization of Quinazolinonyl Enones: a Facile Access to C- Ring Substituted Vasicinones and Luotonins

    A Novel Aza-Nazarov Cyclization of Quinazolinonyl Enones: a Facile Access to C- Ring Substituted Vasicinones and Luotonins

  • The Abnormal Michael Reaction: Scope, Limitations, and Mechanism

    The Abnormal Michael Reaction: Scope, Limitations, and Mechanism

  • Strong and Confined Acids Enable a Catalytic Asymmetric Nazarov

    Strong and Confined Acids Enable a Catalytic Asymmetric Nazarov

  • The Α-Carbon Atom and Its Pka the Inductive Effect of the Carbonyl

    The Α-Carbon Atom and Its Pka the Inductive Effect of the Carbonyl

  • Hydroxy-L-Prolines As Asymmetric Catalysts for Aldol, Michael Addition and Mannich Reactions

    Hydroxy-L-Prolines As Asymmetric Catalysts for Aldol, Michael Addition and Mannich Reactions

  • Translating the Enantioselective Michael Reaction to a Continuous

    Translating the Enantioselective Michael Reaction to a Continuous

  • 1,5 Difunctionalised Compounds, Michael Addition and Robinson Annelation

    1,5 Difunctionalised Compounds, Michael Addition and Robinson Annelation

  • Synthesis and Recovery of Pyridine- and Piperidine-Based Camphorsulfonamide Organocatalysts Used for Michael Addition Reaction

    Synthesis and Recovery of Pyridine- and Piperidine-Based Camphorsulfonamide Organocatalysts Used for Michael Addition Reaction

  • Development of the Conjugate Addition/Nitro-Mannich Reaction

    Development of the Conjugate Addition/Nitro-Mannich Reaction

  • The Chemistry of Enolates and Enols May 3, 2013 • the Acetoacetic and Malonic Ester Syntheses

    The Chemistry of Enolates and Enols May 3, 2013 • the Acetoacetic and Malonic Ester Syntheses

  • Solvent- and Catalyst-Free Aza-Michael Addition of Imidazoles and Related Heterocycles

    Solvent- and Catalyst-Free Aza-Michael Addition of Imidazoles and Related Heterocycles

  • Α-Carbonyl Nucleophiles the Michael Reaction

    Α-Carbonyl Nucleophiles the Michael Reaction

Top View
  • Organocatalysts: a Powerful Tool for Asymmetric Michael Addition
  • Theoretical and Experimental Study of the Regioselectivity of Michael Additions
  • Chem 343 Reactions: Page 1 (You Do Not Need to Know the Mechanism for the Reactions in the Boxes)
  • Lecture Notes Chem 51C S. King Chapter 24 Carbonyl Condensation Reactions I. Reaction of Enols & Enolates with Other Carbo
  • The Logic of Organic Synthesis Semester – Iv Cbcs System
  • Total Synthesis: a Crowning Achievement in Organic Chemistry
  • Introduction 1
  • Catalytic, Enatioselective Michael Addition Reactions
  • Chem 360-Jasperse Chapter 22 (Enolate Chemistry) Reaction Summary
  • Chapter 23. Carbonyl Condensation Reactions
  • Modern Organic Synthesis an Introduction Chapter 1 Synthetic
  • Aldol Condensation
  • Recent Developments in Enantioselective Organocatalytic Michael Reactions in Aqueous Media Helene Pellissier
  • Tetrabutylammonium Bromide Media Aza-Michael Addition of 1,2,3,6-Tetrahydrophthalimide to Symmetrical Fumaric Esters and Acrylic Esters Under Solvent-Free Conditions
  • 1 Chapter 19: Carbonyl Compounds III Learning Objectives: 1. Write the Mechanism for Keto-Enol Tautomerization and Explain the C
  • Michael Additions of Nitroalkanes to Alkenes Activated by Electroattracting Groups in the Presence of Various Basic Systems
  • Metal-Mediated Vinylogous Nazarov Cyclization Reaction
  • 20.10 Conjugate Additions


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