Highly Diastereoselective Michael Addition Reactions of Lithium Enolates to Ethyl 3-Trifluoromethylacrylate
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/20/12/20_12_2171/_pdf
Reference11 articles.
1. Acyclic stereoselection. 46. Stereochemistry of the Michael addition of N,N-disubstituted amide and thioamide enolates to .alpha.,.beta.-unsaturated ketones
2. Acyclic stereoselection. 47. Stereochemistry of the Michael addition of ester and ketone enolates to .alpha.,.beta.-unsaturated ketones
3. A highly stereoselective Michael reaction of simple ester enolates to α,β-unsaturated esters
4. The stereocontrolled construction of the adjacent tertiary carbons by using the Michael addition.
5. Stereochemistry of the Base-Promoted Michael Addition Reaction
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