New allene equivalents for the Diels–Alder reaction: vinyl sulphoxide cycloadditions
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1991/C3/C39910001672
Reference18 articles.
1. Notes- Reactions of Allene. I. Diels-Alder Adducts
2. The Chemistry of Allenes
3. Allene-olefin and allene-allene cycloadditions methylenecyclobutane and 1,2-dimethylenecyclobutane degenerate rearrangements
4. H. F. Schuster and G. M.Coppola, Allenes in Organic Synthesis, Wiley, New York, 1984.
5. Reagent design and study of allene as a promising class of reagents (synthons) for cycloaddition. The site-selective and regioselective Diels-Alder reactions of (phenylsulfonyl)propadiene and alkylation of the adducts
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1. Propargyltrimethylsilanes as Allene Equivalents in Transition Metal-Catalyzed [5 + 2] Cycloadditions;Organic Letters;2014-05-12
2. ChemInform Abstract: New Allene Equivalents for the Diels-Alder Reaction: Vinyl Sulfoxide Cycloadditions.;ChemInform;2010-08-22
3. Phenylsulfinylethylene;Encyclopedia of Reagents for Organic Synthesis;2008-09-15
4. Preparation of Difunctional Compounds;Compendium of Organic Synthetic Methods;2006-11-22
5. Prepackaged Ramberg–Bäcklund reagents: useful tools for organic synthesis;Tetrahedron;2004-08
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