Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1344125 | Tetrahedron: Asymmetry | 2012 | 5 Pages |
Abstract
A reversal in enantioselectivity was observed by the combination of a chiral diol and achiral alcohols as a chiral initiator in the asymmetric alkylation of a pyrimidine-5-carbaldehyde using diisopropylzinc. (2S,3S)-Butane-2,3-diol alone induced (R)-pyrimidyl alkanol, while a mixture of the chiral diol and phenol derivatives induced (S)-pyrimidyl alkanol. The effect of achiral alcohols is also discussed.
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Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Takanori Shibata, Hikaru Tarumi, Tsuneomi Kawasaki, Kenso Soai,