Extremely powerful chiral auxiliaries: Enantiomeric [4+2] cycloadducts of 2-oxazolone and 9,10-dimethylanthracene
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Asymmetric alkylation reactions of chiral imide enolates. A practical approach to the enantioselective synthesis of .alpha.-substituted carboxylic acid derivatives
2. Asymmetric Diels-Alder cycloaddition reactions with chiral .alpha.,.beta.-unsaturated N-acyloxazolidinones
3. Transition Stateπ-Solvation by Aromatic Rings: An Electronic Contribution to Diels–Alder Reaction Diastereoselectivity
4. Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates
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1. Stereoselective Synthesis of 2‐Oxyenamides**;European Journal of Organic Chemistry;2022-08-17
2. An oxazolone cycloadduct approach to Cis-fused decahydroquinoline alkaloids: Regio- & stereocontrolled installation of a C5-substituent by “radical clock”;Tetrahedron Letters;2018-09
3. Formation of Alkenes by Diels-Alder Reactions;Comprehensive Organic Transformations;2018-02-28
4. Cycloadditions II;Key Chiral Auxiliary Applications;2014
5. Alkylation and Related Reactions II;Key Chiral Auxiliary Applications;2014
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