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.
Huvudupphovsmän: | , |
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Materialtyp: | Journal article |
Språk: | English |
Publicerad: |
Royal Society of Chemistry
2007
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Sammanfattning: | DFT computed transition states quantitatively explain the surprising stereochemical outcome of unsubstituted enolborinates in diastereoselective and enantioselective boron aldol reactions. |
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