Control of stereochemistry by sulfoxide chirality in Diels-Alder reactions of 1-methoxy-3-alkylsulfinylbutadienes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
1. Highly diastereoselective Diels-Alder reaction of optically active ethyl 2-p-tolylsulfinylmethylenepropionate with cyclopentadiene
2. Self-induced diastereoselective oxidation of vinyl sulfoxides bearing a chiral hydroxy group as a way of preparation of optically active sulfinyl dienophiles and their use in the asymmetric Diels-Alder reactions to cyclopentadiene
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1. Formation of Alkenes by Diels-Alder Reactions;Comprehensive Organic Transformations;2018-02-28
2. An Asymmetric Redox Arylation: Chirality Transfer from Sulfur to Carbon through a Sulfonium [3,3]-Sigmatropic Rearrangement;Angewandte Chemie International Edition;2017-01-18
3. Asymmetrische Redoxarylierung: Chiralitätstransfer von Schwefel zu Kohlenstoff durch sigmatrope Sulfonium-[3,3]-Umlagerung;Angewandte Chemie;2017-01-18
4. Concise Construction of Bicyclo[6.4.0] and -[7.4.0] Frameworks by [4+2] Cycloaddition of 3,4-Dimethylene-2,5-bis(phenylsulfonyl)cycloalk-1-enes;European Journal of Organic Chemistry;2015-06-02
5. Synthesis of Enantiomerically Pure Bis-Sulfinyl Substituted Phenylene Ethynylenes;Helvetica Chimica Acta;2014-09
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