608137-17-3Relevant academic research and scientific papers
Mukaiyama aldol reaction using ketene silyl acetals with carbonyl compounds in ionic liquids
Chen, Shui-Ling,Ji, Shun-Jun,Loh, Teck-Peng
, p. 375 - 377 (2004)
Mukaiyama aldol reactions using ketene silyl acetals with various aldehydes proceed smoothly in ionic liquids to afford the corresponding aldol products in moderate yields.
Lithium acetate-catalyzed aldol reaction between aldehyde and trimethylsilyl enolate in anhydrous or water-containing N,N-dimethylformamide
Nakagawa, Takashi,Fujisawa, Hidehiko,Nagata, Yuzo,Mukaiyama, Teruaki
, p. 1555 - 1567 (2007/10/03)
Lithium acetate (AcOLi)-catalyzed aldol reactions between trimethylsilyl enolates and aldehydes proceed smoothly in anhydrous DMF or pyridine to afford the corresponding aldols in good to high yields under weakly-basic conditions (Tables 1-5). This cataly
Lithium Acetate Catalyzed Aldol Reaction between Aldehyde and Trimethylsilyl Enolate in a Dimethylformamide-H2O Solvent
Nakagawa, Takashi,Fujisawa, Hidehiko,Mukaiyama, Teruaki
, p. 696 - 697 (2007/10/03)
Lithium acetate catalyzed aldol reaction between trimethylsilyl enolates and aldehydes in a DMF-H2O (50:1) solvent proceeded smoothly to afford the corresponding aldols in good to high yields. It is noted that trimethylsilyl enolates derived fr
