A convenient and stereoselective synthesis of allylic sulfides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference6 articles.
1. Rearrangement and trans-elimination contrary to the chugaev reaction rule. XIII. Solvent effect on rearrangement reaction of allylic xanthates and a correction of the former report.
2. Rearrangement and trans-Elimination contrary to the Chugaev Reaction Rule. VIII. Thermal Rearrangement of 2-Alkenyl S-Alkyl Xanthate
3. Rearrangement and trans-Elimination contrary to the Chugaev Reaction Rule. IX. Thermal Rearrangement of 2-Cycloalkenyl S-Alkyl Xanthate
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1. Carbon-Sulfur Bond Formation via Metal-Catalyzed Allylations of Sulfur Nucleophiles;Synthesis;2013-07-10
2. Synthesis of Neoglycoconjugates by the Desulfurative Rearrangement of Allylic Disulfides;The Journal of Organic Chemistry;2008-08-27
3. Allylic disulfide rearrangement and desulfurization: Mild, electrophile-free thioether formation from thiols;ORG LETT;2006
4. Allylic Disulfide Rearrangement and Desulfurization: Mild, Electrophile-Free Thioether Formation from Thiols;Organic Letters;2006-07-14
5. Cascade Reactions of Unsaturated Xanthates and Related Reactions: Computer-assisted Molecular Design and Analysis of Reaction Mechanisms;YAKUGAKU ZASSHI;2005-06-01
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