Enantioselectivity in the boron aldol reactions of methyl ketones.
DFT computed transition states quantitatively explain the surprising stereochemical outcome of unsubstituted enolborinates in diastereoselective and enantioselective boron aldol reactions.
| Автори: | , |
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| Формат: | Journal article |
| Мова: | English |
| Опубліковано: |
Royal Society of Chemistry
2007
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| Резюме: | DFT computed transition states quantitatively explain the surprising stereochemical outcome of unsubstituted enolborinates in diastereoselective and enantioselective boron aldol reactions. |
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