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.

Opis bibliograficzny
Główni autorzy:	Goodman, J, Paton, R
Format:	Journal article
Język:	English
Wydane:	Royal Society of Chemistry 2007

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