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.

Библиографические подробности
Главные авторы:	Goodman, J, Paton, R
Формат:	Journal article
Язык:	English
Опубликовано:	Royal Society of Chemistry 2007

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