Enantioselective Organocatalysis

Enantioselective organocatalysis has emerged as a potent synthetic paradigm that complements metal-catalyzed reactions and has spurred the development of new ways to create chiral molecules of all shapes and sizes. Organocatalysis is an appealing approach for synthesising complicated structures because of its operational simplicity, ready availability of catalysts, and low toxicity. The impact of enamine, iminium, nucleophilic, and Brnsted acid catalysts in organic synthesis is discussed in this paper, as well as crucial strategic strategies for assembling useful compounds with high enantiomeric purity.

 

Sub-Tracks

  • Aldol reactions
  • Mannich-type transformations
  • Substitution reactions
  • Animation, hydroxylation and aminoxylation reactions
  • Asymetric conjugate additions
  • Allylation reactions
  • Cycloaddition reactions
  • Acylation reactions
  • Hydrocyanation of carbonyl compounds and imines
  • Reduction of carbonyl compounds and olefins
  • Oxidation reactions
  • Ylide-based reactions: aziridination, epoxidation and cyclopropanation

Tags
Organic Chemistry Conferences European Chemistry Conferences 2025 Medicinal Chemistry Conferences Chemistry Conferences 2025 Chemistry Conferences 2025 Biochemistry Conferences Inorganic Chemistry Conferences Computational Chemistry Conferences International Chemistry Conferences Materials Science Conferences Food Chemistry Conferences Geochemistry Conferences 2025 Food Chemistry Conferences 2025 Industrial Chemistry Conferences Organic Chemistry Conference, Meetings 2025

+1 (506) 909-0537