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.

Dades bibliogràfiques
Autors principals:	Goodman, J, Paton, R
Format:	Journal article
Idioma:	English
Publicat:	Royal Society of Chemistry 2007

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