Cycloadditions of Allyl Cations, 26 1) Norbornene Derivatives from Cyclopentadiene and 2,4‐Dimethyl‐3‐penten‐2‐ol in an Acidic Two Phase System. A Stepwise Diels‐Alder‐like Cyclization
Author:
Affiliation:
1. Institut für Organische Chemie, Universität Hannover, Schneiderberg 1B, D‐3000 Hannover
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19811140423
Reference13 articles.
1. Cycloadditions of allyl cations, 25. Acid catalyzed dehydrative cyclodimerization of 2,4‐dimethyl‐3‐penten‐2‐ol in two phases. Biomimetic one‐pot preparation of 3,3,5,5‐tetramethyllimonene (4‐isopropenyl‐1,3,3,5,5‐pentamethyl‐1‐cyclohexene)
2. Synthese von Norbornen-Derivaten aus Cyclopentadien und Allylalkoholen in einem sauren Zweiphasensystem
3. Synthesis of Norbornenes from Cyclopentadiene and Allyl Alcohols in an Acidic Two Phase System
4. Cycloadditions of allyl cations, 22. Allyl alcohols as precursors of allyl cations
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1. Diels–Alder reactions of 1,1,3-triarylallyl cations: determination of the free energy of concert;J. Chem. Soc., Perkin Trans. 2;2002
2. Stereochemistry in the Ene Reactions of Singlet Oxygen and Triazolinediones with Allylic Alcohols. A Mechanistic Comparison;The Journal of Organic Chemistry;1999-05-01
3. Solvent effects in the stereoselectivity of the ene reaction of singlet oxygen with allylic alcohols;Tetrahedron Letters;1996-09
4. Zirconocene-catalyzed cationic Diels-Alder reactions;Tetrahedron;1995-04
5. Transition Metal Carbene Complexes: Tebbe’s Reagent and Related Nucleophilic Alkylidenes;Comprehensive Organometallic Chemistry II;1995
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