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CHEM-647 (Organic Synthesis)
Specific enolate equivalents
Specific enolate equivalents
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specific-enolate-equivalent-1.pdf (2.70 MB )
specific-enolate-equivalent-2.pdf (1.95 MB )
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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