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123.312 Retrosynthesis: lecture 5
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123.312 Retrosynthesis: Lecture 3
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This is an experiment. It is NOT a presentation. It is meant to be an interactive pdf for students to work through/revise from at their own pace. For these features to operate I guess it needs to be downloaded first. It is based on 123.312 lectures on retrosynthesis or the design of chemical syntheses.
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This is an experiment. It is NOT a presentation. It is meant to be an interactive pdf for students to work through/revise from at their own pace. For these features to operate I guess it needs to be downloaded first. It is based on 123.312 lectures on retrosynthesis or the design of chemical syntheses.
Retrosynthesis: 123.312
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Lecture6: 123.312
Lecture6: 123.312
Gareth Rowlands
Told you that this was the important one. This weeks reagents include more enolates and then reactions with the C=O group including the such classics as the Wittig reaction.
Lecture7: 123.312
Lecture7: 123.312
Gareth Rowlands
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Lecture2: 123.312
Lecture2: 123.312
Gareth Rowlands
Finishing oxidation by looking at the Baeyer-Villiger reaction and then turning our attention to reduction. Once again we will see the usual suspects with a who is who of hydride sources.
Lecture5: 123.312
Lecture5: 123.312
Gareth Rowlands
A brief look at alcohol protecting groups and then an introduction to carboxylic acid derivatives. Start of the reactions of carboxylic acids.
Lecture3: 123.312
Lecture3: 123.312
Gareth Rowlands
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Lecture 8: the aldol reaction and conjugate additions Just what it says in the title.
Lecture8: 123.312
Lecture8: 123.312
Gareth Rowlands
Finishing off the reactions of carboxylic acid derivatives (well the substitution reactions) and introducing oxidation and reduction. Then looking at the oxidation of alkenes (epoxidation and dihydroxylation) and alcohols (the usual suspects).
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Lecture4: 123.312
Gareth Rowlands
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Tutorial 1 answers
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Gareth Rowlands
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Lecture3 123713B
Gareth Rowlands
More problems covering asymmetric synthesis. This time with examples of substrate control, chiral reagents, and chiral catalysis. Also another example of a synthesis.
Problems 2 answers
Problems 2 answers
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Chiral catalysis. This is a relatively brief look at some classic examples of chiral catalysis in organic synthesis. It gives a quick overview but does not go into any detail.
Lecture2 123713A
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The second set of tutorial questions on asymmetric synthesis. This one covers chiral reagents and starts enantioselective catalysis.
Tutorial 2 answers
Tutorial 2 answers
Gareth Rowlands
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Lecture4: 123.702
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Lecture6: 123.702
Gareth Rowlands
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Lecture9:123.702
Lecture9:123.702
Gareth Rowlands
More substrate control, including allylic strain and directed reactions.
Lecture2: 123.702
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Gareth Rowlands
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Basic Concepts Of Retrosynthesis (Part1)
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Lecture6: 123.312
Lecture7: 123.312
Lecture7: 123.312
Basic Concepts Of Retrosynthesis (Part 2)
Basic Concepts Of Retrosynthesis (Part 2)
Lecture2: 123.312
Lecture2: 123.312
Lecture5: 123.312
Lecture5: 123.312
Lecture3: 123.312
Lecture3: 123.312
Problems 1 answers
Problems 1 answers
Lecture8: 123.312
Lecture8: 123.312
Lecture4: 123.312
Lecture4: 123.312
Tutorial 1 answers
Tutorial 1 answers
Lecture3 123713B
Lecture3 123713B
Problems 2 answers
Problems 2 answers
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Lecture2 123713A
Tutorial 2 answers
Tutorial 2 answers
Lecture4: 123.702
Lecture4: 123.702
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Lecture6: 123.702
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Lecture9:123.702
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