Säurekatalysierte Cyclodimerisierungen über Vinylkationen als Zwischenstufen
- 1 December 1969
- journal article
- research article
- Published by Wiley in Angewandte Chemie
- Vol. 81 (23) , 966-970
- https://doi.org/10.1002/ange.19690812303
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Preparation and solvolysis of vinyl trifluoromethanesulfonates. I. Evidence for simple alkylvinyl cation intermediatesJournal of the American Chemical Society, 1969
- Unsaturated neopentyl compounds. The effect of methyl substitution on the acetolysis rates of homoallenic neopentyl-type brosylatesJournal of the American Chemical Society, 1969
- Anchimeric assistance, rearrangement, and solvent addition in the formolysis of a nonconjugated acetylenic (homopropargylic) tosylateJournal of the American Chemical Society, 1969
- Vinyl cation. Solvolysis of 1-cyclopropyl-1-chloroethyleneJournal of the American Chemical Society, 1969
- Synthesis and solvolysis of 1-cyclopropyl-1-iodoethylene. Generation of an unusually stable vinyl cationJournal of the American Chemical Society, 1969
- Solvolysis of triaryliodoethylenes. Structure and selectivity of vinyl cationsJournal of the American Chemical Society, 1968
- Polar Additions to Olefins and Actylenes. III. The Kinetics and Stereochemistry of Addition in the System 1-Phenylpropyne-Hydrogen Chloride-Acetic Acid1Journal of the American Chemical Society, 1966
- Concerning the Acid-Catalyzed Hydration of AcetylenesJournal of the American Chemical Society, 1965
- Nitrosation Reactions of Primary Vinylamines. Possible Divalent Carbon Intermediates1Journal of the American Chemical Society, 1965
- Die Solvolyse von α‐Bromstyrolen Substitution am ungesättigten trigonalen KohlenstoffatomHelvetica Chimica Acta, 1964