Synthesis and diels-alder reactions of (S)-3-chloro and (S)-3-ethyl-2-p-tolylsulfinyl-1,4-benzoquinones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Synthesis and asymmetric diels-alder reactions of (S)-2-p-tolylsulfinyl-1,4-benzoquinone
2. Asymmetric Diels-Alder reactions of (S)-2-(p-tolylsulfinyl)-1,4-naphthoquinones
3. Benzyl Methyl (S)-2-(p-Tolylsulfinyl)maleate, an Efficient Dienophile in Asymmetric Diels-Alder Reactions
4. Powerful dienophiles for asymmetric Diels-Alder reactions: .alpha.-(2-exo-hydroxy-10-bornylsulfinyl)maleimides
5. Chiral epoxides as recoverable auxiliaries in the synthesis of optically active sulpinyl dienophiles
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2. ChemInform Abstract: Synthesis and Diels-Alder Reactions of (S)-3-Chloro and (S)-3-Ethyl-2- p-tolylsulfinyl-1,4-benzoquinones.;ChemInform;2010-08-18
3. Studies on chemo- and diastereo-selectivity of the Diels–Alder reactions of sulfinyltoluquinones with cyclopentadiene;Canadian Journal of Chemistry;2009-08
4. One-Step versus Stepwise Mechanism in Protonated Amino Acid-Promoted Electron-Transfer Reduction of a Quinone by Electron Donors and Two-Electron Reduction by a Dihydronicotinamide Adenine Dinucleotide Analogue. Interplay between Electron Transfer and Hydrogen Bonding;Journal of the American Chemical Society;2008-04-01
5. The chemistry of sulfinyl and sulfonyl enones;Tetrahedron;2007-12
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