Reversal of Polarity, Cyclizations, Summary of Strategies
B. Important Reactions used in WW Chapter 7:
Synthesis of 1,2-DiX electrophiles
-chloroperbenzoic acid (MCPBA)
-chloroperbenzoic acid (MCPBA)
The products in reactions a-e are starting materials revealed in the 2-Group Di-X activity. Now we are exploring how they can be synthesized and the
nature of their reactivity:
1. Identify the 1,2-DiX relationships in each product above.
2. Identify the potentially electrophilic site(s) in each product.
3. WW refers to these reagents as ones with “reversal of polarity”. Compare the reactivity of the carbon atoms identified in 2 in the products to
the reactivity of the same carbon atom in the reactants of a-e and explain what the authors mean by “reversal of polarity”.
Summary of Strategies for Retroanalysis
This section is a review of the strategies we have been discovering so far this semester. Most is review, but the consideration of cyclizations has not been emphasized previously. (Compare these lists to the ones in WW Chapter 1, p. 4) WW illustrates some of the strategies with a discussion of the synthesis of Salbutamol.
1. Recognize the functional groups in the target molecule.
2. Disconnect by known reliable methods using FGI's if necessary to produce the best functional groups for disconnections.
3. Best disconnections to look for first are:
a. Bonds joining an aromatic ring to the rest of the molecule. (Aromatic Compounds 1 & 2 Activities and WW Chapters 2&3) b. Any C-X disconnections especially:
(1) Bonds next to carbonyl groups. (Acyl C-X, 1 Group C-X activity and WW Chapter 4) (2) 2-group C-X disconnections of 1,1-, 1,2- or 1,3- systems. (2-Group Di-X Activity and WW Chapter 6) (3) C-X disconnections of bonds within rings because cyclizations are favorable. (WW Chapter 7)
Recall the syntheses of the compounds below from the 2-Group Di-X activity.
4. Repeat as necessary to reach available starting materials.
Conversion of a Retrosynthetic Analysis to a Synthetic Scheme
Write out the plan according to the retrosynthetic scheme, adding relevant reagents and reaction conditions.
Check that a rational order of events has been chosen. (See guidelines from Model 4 of Aromatic Compound 2 Activity and WW Chapter 3)
Check that Chemoselectivity is favorable (See Chemoselectivity Guidelines Activity and WW Chapter 5). Use protecting groups if necessary. (WW Chapter 9)
Modify the planned synthesis to correct for problems detected in #'s 2 & 3 above.
In our first activity “Summary of Retrosynthetic Approach to Organic Synthesis”
we explored a retrosynthetic analysis of multistriatin and
converted one of the retrosynthetic branches into a synthesis. In chapter 1, WW discusses the retrosynthetic analysis of multistriatin but follows a
branch that is somewhat different from the ones we used in the first activity. Also, in our first couple of classes, we had few tools to allow us to
engage in the retroanalysis. So our application for this activity is to:
1. Write out the retrosynthetic analysis for multistriatin described in WW chapter 1, pp. 2 & 3, and identify the disconnections they used and other
potential 2-Group-DiX disconnections they might have used. Then indicated how the “Summary of Strategies for Retroanalysis”
(p. 2 and
Chapter 7) were used or ignored in the retroanalysis.
2. Analyze the synthesis that they developed from the retroanalysis. (WW p. 4) Indicate how it deviated from the retroanalysis and how it does or
does not illustrate the “Conversion of a Retrosynthesis to a Synthetic Scheme”
Après une formation de plusieurs années au conservatoire de musique de Genève, la pianiste Valérie Blanvillain obtient le premier prix à l’unanimité au Concours International Claude Debussy à Lyon. En parallèle, elle obtient en son diplôme de musicothérapeute et travaille pendant 6 ans en clinique psychiatrique et en maison de retraite. Elle parfait sa formation pianistiq
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