A Convenient Method for Conversion of Allylic Chlorides to α,β-Unsaturated Aldehydes
- 1 October 1986
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 59 (10) , 3287-3288
- https://doi.org/10.1246/bcsj.59.3287
Abstract
Tertiary amine N-oxides were found to be effective for converting allylic chlorides to α,β-unsaturated aldehydes.This publication has 6 references indexed in Scilit:
- Regio- and Stereoselective Oxidation of Ene-Type Chlorinated OlefinsSynthetic Communications, 1985
- New Synthetic Method for Bicyclic Compounds Through a Sequence of Ene-Type Chlorination, Palladium Catalyzed Dehydrochlorination, and Intramolecular Diels-Alder ReactionSynthetic Communications, 1984
- Facile synthesis of 4-acetoxy-2-methyl-2-butenal, a vitamin A precursor, from isoprene chlorohydrinThe Journal of Organic Chemistry, 1979
- Eine neue Methode zur Darstellung von CarbonylverbindungenEuropean Journal of Inorganic Chemistry, 1961
- Communications - Alkaline Decomposition of Quaternary Salts of Amine OxidesThe Journal of Organic Chemistry, 1957
- Synthesen in der Carotinoid‐Reihe. 11. Mitteilung. α,β‐Ungesättigte Carbonylverbindungen aus Allylhalogeniden mittels NitroparaffinenHelvetica Chimica Acta, 1957