Tetrahedron Letters p. 2947 - 2950 (1999)
Update date:2022-08-11
Topics:
Schmitzer
Perez
Rico-Lattes
Lattes
Sodium borohydride reduced, at the chiral interface of an amphiphilic dendrimer, prochiral ketones to the corresponding chiral alcohols in high yields (>90%) with enantioselectivities over 95% in THF (ex: ee of 99.4% was obtained in reduction of acetophen
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