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.

Detaylı Bibliyografya
Asıl Yazarlar:	Goodman, J, Paton, R
Materyal Türü:	Journal article
Dil:	English
Baskı/Yayın Bilgisi:	Royal Society of Chemistry 2007

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