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.
Hoofdauteurs: | , |
---|---|
Formaat: | Journal article |
Taal: | English |
Gepubliceerd in: |
Royal Society of Chemistry
2007
|
Samenvatting: | DFT computed transition states quantitatively explain the surprising stereochemical outcome of unsubstituted enolborinates in diastereoselective and enantioselective boron aldol reactions. |
---|