## Abstract The asymmetric aldol‐Tishchenko reaction of aromatic aldehydes with aliphatic and aromatic ketones has been developed as an efficient strategy for the synthesis of __anti__‐1,3‐diols in good yield with high diastereocontrol and good levels of enantioselectivity. This domino‐type reactio
Chiral Ytterbium Complex-Catalyzed Direct Asymmetric Aldol—Tishchenko Reaction: Synthesis of anti-1,3-Diols.
✍ Scribed by Jacek Mlynarski; Bartosz Rakiel; Maciej Stodulski; Agata Suszczynska; Jadwiga Frelek
- Publisher
- John Wiley and Sons
- Year
- 2007
- Weight
- 28 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0931-7597
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1997 carboxylic acid esters carboxylic acid esters (benzene compounds) Q 0530 35 -098 Enantioselective Acyclic Stereoselection under Catalyst Control. Part 2. Asymmetric Synthesis of syn-and anti-1,3-Diols Incorporating an Acetate Equivalent by the Chiral Oxazaborolidinone-Catalyzed Aldol Reaction.