Threo selective cross aldol condensation with thioamide enolates generated by a michael addition of organometallics to unsaturated thioamides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Stereoselective generation of Z-enolates of thioamides: its application to diastereoselective aldol condensations and thio-Claisen rearrangements
2. Stereoselective generation of (Z)-secondary thioamide dianion: application to diastereoselective aldol condensations and thio-Claisen rearrangements
3. Acyclic stereoselection. 4. Assignment of stereostructure to .beta.-hydroxycarbonyl compounds by carbon-13 nuclear magnetic resonance
4. Observations on the stereochemistry of aldol reaction products. Crystal and molecular structure of erythro-4-(benzoyloxy)-3-tert-butyl-4-phenylbutan-2-one
5. See accompanying communication.
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