Enantioselective aldol reaction using bornane-2,3-diol-aluminum complex as a chiral Lewis acid

DOI: 10.1055/s-1997-6148

Source and publish data:

Synlett p. 501 - 502 (1997)

Update date:2022-08-05

Topics:

Authors:

Shimizu, Makoto

Kawamoto, Manabu

Yamamoto, Yasushi

Fujisawa, Tamotsu

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Article abstract of DOI:10.1055/s-1997-6148

β-Hydroxy ester was formed in high enantiomeric excess by the reaction of ketene silyl acetal with aldehyde in the presence of a chiral Lewis acid prepared from diethylaluminum chloride and chiral diol derived from (+)-camphor.

Full text of DOI:10.1055/s-1997-6148

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