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.

Dettagli Bibliografici
Autori principali:	Goodman, J, Paton, R
Natura:	Journal article
Lingua:	English
Pubblicazione:	Royal Society of Chemistry 2007

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