Journal
ORGANIC LETTERS
Volume 16, Issue 3, Pages 944-947Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol4036837
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Funding
- MEXT, Japan
- Japan Society for the Promotion of Science
- Grants-in-Aid for Scientific Research [26220803] Funding Source: KAKEN
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Various heterofunctionalized acetaldehydes were successfully employed in an amine-catalyzed asymmetric cross-aldol reaction, affording a variety of synthetically useful 1,2-difunctionalized compounds such as 1,2-diols and 1,2-aminoalcohols. With this method, both syn- and anti-1,2-difunctionalized compounds were obtained from the same set of reactants by using the appropriate amine catalyst.
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