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.

Sonraí bibleagrafaíochta
Príomhchruthaitheoirí: Goodman, J, Paton, R
Formáid: Journal article
Teanga:English
Foilsithe / Cruthaithe: Royal Society of Chemistry 2007
Cur síos
Achoimre:DFT computed transition states quantitatively explain the surprising stereochemical outcome of unsubstituted enolborinates in diastereoselective and enantioselective boron aldol reactions.