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Organic Synthesis and
Retro-synthesis:
Fundamentals
Essential Concepts for Success
By:Ali Hamza
Organic Chemistry 8TH Semester
Introduction
•Definition of Organic Synthesis: The art of building
organic molecules from simpler starting materials.
•Importance: Essential for drug discovery, materials
science, and understanding biological processes.
•Objective: To understand the principles of retrosynthesis
and apply them to design synthetic routes.
Key Terminology
•Organic molecule: Carbon-based compounds containing
hydrogen and other elements.
•Functional group: A specific arrangement of atoms
responsible for the characteristic chemical reactions of a
compound.
•Retrosynthesis: The process of breaking down a target
molecule into simpler precursor molecules.
Functional Group Analysis
•Overview of common functional groups: Alkanes,
alkenes, alkynes, alcohols, ethers, aldehydes, ketones,
carboxylic acids, esters, amines, amides.
•Importance of functional groups in synthesis planning.
Retrosynthetic Analysis
•Definition: Breaking down a target molecule into simpler,
readily available starting materials.
•Disconnection: Identifying bonds to be made and bonds
to be broken.
•Retrosynthetic arrow: Representing disconnections in a
synthetic pathway.
Strategic Bond Disconnections
•Introduction to common disconnection strategies:
Functional group interconversions, carbon-carbon bond
cleavage, carbon-heteroatom bond formation.
•Example reactions for each strategy.
Synthetic Equivalents
•Definition: Functional groups or molecules that can be
interconverted through a specific reaction.
•Importance of choosing appropriate synthetic equivalents
for efficient synthesis.
Synthesis Planning
•Putting it all together: Applying retrosynthetic analysis to
plan synthetic routes.
•Importance of step economy, yield, and feasibility.
Stereochemistry in Synthesis
•Overview of stereochemistry: Chirality, enantiomers,
diastereomers.
•Importance of stereochemical control in synthesis.
Conclusion
•Recap of key points: Functional groups, retrosynthesis,
synthesis planning, strategic disconnections, synthetic
equivalents, stereochemistry.
•Importance of mastering these fundamentals for success
in organic synthesis.
•Encouragement for further exploration and practice.

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Organic Synthesis and Retro-synthesis.pptx

  • 1. Organic Synthesis and Retro-synthesis: Fundamentals Essential Concepts for Success By:Ali Hamza Organic Chemistry 8TH Semester
  • 2. Introduction •Definition of Organic Synthesis: The art of building organic molecules from simpler starting materials. •Importance: Essential for drug discovery, materials science, and understanding biological processes. •Objective: To understand the principles of retrosynthesis and apply them to design synthetic routes.
  • 3. Key Terminology •Organic molecule: Carbon-based compounds containing hydrogen and other elements. •Functional group: A specific arrangement of atoms responsible for the characteristic chemical reactions of a compound. •Retrosynthesis: The process of breaking down a target molecule into simpler precursor molecules.
  • 4. Functional Group Analysis •Overview of common functional groups: Alkanes, alkenes, alkynes, alcohols, ethers, aldehydes, ketones, carboxylic acids, esters, amines, amides. •Importance of functional groups in synthesis planning.
  • 5. Retrosynthetic Analysis •Definition: Breaking down a target molecule into simpler, readily available starting materials. •Disconnection: Identifying bonds to be made and bonds to be broken. •Retrosynthetic arrow: Representing disconnections in a synthetic pathway.
  • 6. Strategic Bond Disconnections •Introduction to common disconnection strategies: Functional group interconversions, carbon-carbon bond cleavage, carbon-heteroatom bond formation. •Example reactions for each strategy.
  • 7. Synthetic Equivalents •Definition: Functional groups or molecules that can be interconverted through a specific reaction. •Importance of choosing appropriate synthetic equivalents for efficient synthesis. Synthesis Planning •Putting it all together: Applying retrosynthetic analysis to plan synthetic routes. •Importance of step economy, yield, and feasibility. Stereochemistry in Synthesis •Overview of stereochemistry: Chirality, enantiomers, diastereomers. •Importance of stereochemical control in synthesis.
  • 8. Conclusion •Recap of key points: Functional groups, retrosynthesis, synthesis planning, strategic disconnections, synthetic equivalents, stereochemistry. •Importance of mastering these fundamentals for success in organic synthesis. •Encouragement for further exploration and practice.