Sequential pericyclic reaction of unsaturated xanthates. Intramolecular cycloaddition selectivity of the 2,4-alkadienyl 2-alkenyl sulfides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. A convenient and stereoselective synthesis of allylic sulfides
2. Stereoselective formation of allylic sulfides via two sequential (3,3)-sigmatropic rearrangements of allylic xanthates and its mechanistic aspects.
3. Retro-ene type fragmentation of allylic dithiolcarbonates
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1. Formation Mechanism of Furfuryl Sulfides from O-Furfuryl Dithiocarbonates: Density Functional Theory Study for Aromatic [3,3]-Sigmatropic Rearrangement;Chemical and Pharmaceutical Bulletin;2011
2. ChemInform Abstract: Sequential Pericyclic Reaction of Unsaturated Xanthates. Intramolecular Cycloaddition Selectivity of the 2,4-Alkadienyl 2- Alkenyl Sulfides.;ChemInform;2010-08-04
3. Cascade Reactions of Unsaturated Xanthates and Related Reactions: Computer-assisted Molecular Design and Analysis of Reaction Mechanisms;YAKUGAKU ZASSHI;2005-06-01
4. The Diels-Alder reaction: an update;Journal of the Brazilian Chemical Society;2001-10
5. A Theoretical Study of Neighboring-Group Participation in Thione-to-Thiol Rearrangement of Xanthates. Molecular Orbital Calculation Using a Conductor-Like Screening Model (COSMO) Approach.;Chemical and Pharmaceutical Bulletin;2001
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