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Protecting groups |
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| Mar17-13, 08:14 PM | #1 |
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Protecting groups
Hello,
I am unsure of how to utilize protecting groups in organic synthesis problems. What would be an immediate sign to the trained eye that one should use a protecting group such as TBDMS-Cl? |
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| Mar17-13, 09:28 PM | #2 |
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What is the purpose of protecting groups (PG)?
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| Mar17-13, 09:57 PM | #3 |
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To protect something from being reduced completely
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| Mar17-13, 10:05 PM | #4 |
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Protecting groups
Look for an alcohol that you want to keep in addition to a carbonyl that you want to reduce
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| Mar17-13, 11:03 PM | #5 |
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Here is wiki's list of functional groups and their protecting groups: http://en.wikipedia.org/wiki/Protecting_group When I see TBDMS-Cl, I see a radical Cl anion waiting to react with an acidic hydrogen,usually in a hydroxyl group. |
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