Electron-Donating and -Accepting Strength of Enoxysilanes and Allylsilanes in the Reaction with Aldehydes
Author:
Affiliation:
1. Contribution from the Division of Molecular Engineering, Kyoto University, Kyoto 606-01, Japan
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja963677o
Reference56 articles.
1. New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride
2. Asymmetric aldol reaction between achiral silyl enol ethers and achiral aldehydes by use of a chiral promoter system
3. Catalytic asymmetric aldol reactions. Use of a chiral (acyloxy)borane complex as a versatile Lewis-acid catalyst
4. Enantioselective chiral borane-mediated aldol reactions of silyl ketene acetals with aldehydes. The novel effect of the trialkysilyl group of the silyl ketene acetal on the reaction course
5. New catalysts for the asymmetric aldol reaction: chiral boranes prepared from .alpha.,.alpha.-disubstituted glycine arenesulfonamides
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