Enantioselectivity in the boron aldol reactions of methyl ketones.

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.

Bibliografiset tiedot
Päätekijät:	Goodman, J, Paton, R
Aineistotyyppi:	Journal article
Kieli:	English
Julkaistu:	Royal Society of Chemistry 2007

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