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CHEM-647 (Organic Synthesis)
Specific enolate equivalents

Specific enolate equivalents

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Course Material
  • Introduction and importance of Organic Synthesis. Methods for C – C bond formation, Methods for generation of carbanions
  • Enolate chemistry for C – C bond formation, Role of medium in alkylation reactions
  • Kinetic vs Thermodynamic enolat, O vs C-alkylation
  • Specific enolate equivalents
  • Michael addition, Mannich Reaction and Robinson annulation
  • Ylides in C-C bond formation. Concept of Umpolung
  • Methods for C–O, C – N bond formation, Trends in organic synthesis
  • Introduction and role of protective groups in organic synthesis, Protective groups for carbonyl, alcohols and amines functionalities
  • Mid Term Exam
  • Introduction to reterosynthesis, concept of 1,1, 1,2 disconnections, Functional group inter-conversion (FGI)
  • Disconnections of alcohols and its derivatives
  • Disconnections of alkenes
  • Disconnections of saturated hydrocarbons
  • Retrosynthesis of difunctionalized compounds
  • Disconnections of 1,3-dioxygenated compounds
  • Disconnections of carboxylic acids and simple carbonyl compounds
  • Disconnections of 1,5-dicarbonyls
  • Practice and exercise of retrosynthesis as well as synthesis of multifunctional organic compounds
  • Chapters 18
  • Department Chemistry
  • Teacher Dr. Humaira Yasmeen Gondal
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