The use of two optically active N-sulfinyl α-imino esters in the stereoselective aza-Diels–Alder reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference59 articles.
1. For examples of the diastereoselective aza-Diels–Alder reactions with chiral imines, see:
2. Carbohydrates as Chiral Templates: Stereoselective Tandem Mannich-Michael Reactions for the Synthesis of Piperidine Alkaloids
3. Amino Acid Esters as Chiral Auxiliary Groups in Lewis Acid Catalyzed Reactions of Electron-rich Siloxydienes with Imines
4. Asymmetric aza Diels-Alder reactions of amino acid ester imines with Brassard's diene
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