Indium-trichloride catalyzed mukaiyama-aldol reaction in water: Solubility, aggregation and internal pressure effect
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G. Cao | T. Loh | Jian Pei | Xu-ran Li | Kevin Siong-Ve Koh
[1] Shuj Kobayashi,et al. Lanthanide triflates as water-tolerant Lewis acids. Activation of commercial formaldehyde solution and use in the aldol reaction of silyl enol ethers with aldehydes in aqueous media , 1994 .
[2] A. Lubineau,et al. Water-promoted organic reactions. aldol reaction of silyl enol ethers with carbonyl compounds under atmospheric pressure and neutral conditions. , 1989 .
[3] André Lubineau,et al. Water-promoted organic reactions: aldol reaction under neutral conditions , 1986 .
[4] P. Grieco,et al. “Micellar” catalysis in the aqueous intermolecular diels-alder reaction: rate acceleration and enhanced selectivity , 1983 .
[5] Ronald Breslow,et al. Hydrophobic acceleration of Diels-Alder reactions , 1980 .
[6] Charles Tanford,et al. The hydrophobic effect , 1980 .
[7] Kazuo Banno,et al. New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride , 1974 .