Cycloadditions of Allyl Cations, 29. Acid Catalyzed Reactions of 2,3‐Dimethyl‐3‐penten‐2‐ol and Cyclopentadiene in Two Phases. Formation of Seven‐ and Five‐membered Rings-Reference-Cited by-同舟云学术

Cycloadditions of Allyl Cations, 29. Acid Catalyzed Reactions of 2,3‐Dimethyl‐3‐penten‐2‐ol and Cyclopentadiene in Two Phases. Formation of Seven‐ and Five‐membered Rings

Published:1981-08 Issue:8 Volume:114 Page:2898-2906
ISSN:0009-2940
Container-title:Chemische Berichte
language:en
Short-container-title:Chem. Ber.

Author:

Hoffmann H. M. R.¹,Vathke‐Ernst Heidrun¹

Affiliation:

1. Institut für Organische Chemie der Universität Hannover, Schneiderberg 1 B, D‐3000 Hannover

Publisher

Wiley

Subject

Inorganic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19811140820

Reference17 articles.

1. Cycloadditions of Allyl Cations, 28 1) Novel Diels‐Alder Additions via Acid Catalyzed Reactions of 4‐Methyl‐3‐penten‐2‐ol with Cyclopentadiene and Cyclohexadiene in Two Phases. Formation of Monocyclic, Bicyclic, and Tricyclic Adducts and Double Fragmentation of a Norbornenylcarbinol

2. 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)

3. 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

4. Synthese von Norbornen-Derivaten aus Cyclopentadien und Allylalkoholen in einem sauren Zweiphasensystem

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