Stereodivergent Diels-Alder Reactions Employing Cyclitols as Chiral Auxiliaries
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/24/11/24_11_975/_pdf
Reference19 articles.
1. Development of selective synthetic processes leading to fine chemicals. - Diastereofacial control in the nucleophilic addition to carbonyl compounds.
2. Creation of chirality in the reaction of the chiral ester enolate-imine condensation leading to the stereodivergent synthesis of β-lactams
3. Diastereoface-discriminative metal coordination in asymmetric synthesis: D-pantolactone as practical chiral auxiliary for Lewis acid catalyzed Diels-Alder reactions
4. (S)-Proline benzyl ester as chiral auxiliary in Lewis acid catalyzed asymmetric Diels-Alder reactions
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1. Cycloadditions II;Key Chiral Auxiliary Applications;2014
2. ChemInform Abstract: Stereodivergent Diels-Alder Reactions Employing Cyclitols as Chiral Auxiliaries.;ChemInform;2010-08-12
3. Total syntheses of cyclitol based natural products from myo-inositol: brahol and pinpollitol;Tetrahedron;2009-05
4. Chiral linker 5: scope and limitations of arylsubstituted m-hydrobenzoins as solid supported open chain chiral auxiliaries for diastereoselective syntheses;Tetrahedron: Asymmetry;2009-02
5. Enantioselective Diels-Alder Reactions: Effect of the Achiral Template on Reactivity and Selectivity;Synlett;2007-02
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