Solvent Assisted Oxy-Cope Rearrangement of Diastereomeric 1,5-Hexaden-3-ols. A New Industrial Process for Polyprenyl Ketones
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/52/7/52_7_1983/_pdf
Reference14 articles.
1. �ber eine neuartige Synthese von ?-Ketoallenen durch Reaktion von terti�ren Acetylencarbinolen mit Vinyl�thern eine ergiebige methode zur darstellung des Pseudojonons und verwandter verbindungen
2. �ber die Reaktion von terti�ren Vinylcarbinolen mit Isopropenyl�ther Eine neue Methode zur Herstellung von ?, ?-unges�ttigten Ketonen
3. Addition of a functionalized isoprene unit to an allyl alcohol. I. The synthesis of .beta.-sinensal and related topics
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1. Quantitative Measures of Solvent Polarity;Chemical Reviews;2004-01-01
2. High-Rate Accelerations in Oxy-Cope Rearrangements Induced by Sulfur Substitution: Kinetic Study Involving Electronically and Geometrically Differentiated 1-Alkenyl-2-(Z-1-propenyl)-7,7-dimethyl-exo-norbornan-2-ols;Journal of the American Chemical Society;2000-10-11
3. Photophysical Characterization of Sulfonated Aluminum Phthalocyanines in a Cationic Reversed Micellar System;Langmuir;1996-01-01
4. Cope, Oxy-Cope and Anionic Oxy-Cope Rearrangements;Comprehensive Organic Synthesis;1991
5. Effect of alkyl substituents in 1,5-dien-3-ols on low-temperature sigmatropic [3,3] rearrangement catalyzed by palladium(II) complexes;Bulletin of the Academy of Sciences of the USSR Division of Chemical Science;1987-01
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