Diastereoselective Addition of Organometallics to α-Keto Esters Bearingchiro-Inositol Derivatives as Chiral Auxiliaries
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/21/3/21_3_447/_pdf
Reference13 articles.
1. Asymmetric synthesis of functionalized tertiary homoallyl alcohols by diastereoselective allylation of chiral .alpha.-keto amides derived from (S)-proline esters: control of stereochemistry based on saturated coordination of Lewis acid
2. Application de reactions d'hydroalumination en synthese organique: obtention d'α-alkyl α-hydroxyesters par addition enantioselective de tetraalkylaluminates AU phenylglyoxalate de (−) menthyle.
3. Development of selective synthetic processes leading to fine chemicals. - Diastereofacial control in the nucleophilic addition to carbonyl compounds.
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1. Enantioselective addition of organozinc reagents to carbonyl compounds catalyzed by a camphor derived chiral γ-amino thiol ligand;Tetrahedron;2016-05
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