Functionalization of Isophorone Involving Polychlorination. Part II: Chlorination of Isophorone in the 2- and 6-Position Involving Addition of Chlorine to the Double Bond. Enol Allyl Rearrangements and Base-Induced Substitution of the 6-Chloro Atom-Reference-Cited by-同舟云学术

Functionalization of Isophorone Involving Polychlorination. Part II: Chlorination of Isophorone in the 2- and 6-Position Involving Addition of Chlorine to the Double Bond. Enol Allyl Rearrangements and Base-Induced Substitution of the 6-Chloro Atom

Published:2010-09-01 Issue:9 Volume:96 Page:663-674
ISSN:0037-9646
Container-title:Bulletin des Sociétés Chimiques Belges
language:en
Short-container-title:Bull. Soc. Chim. Belges

Author:

De Buyck L.,Bostoen R.,Lecluse M.,De Pooter H.,Schamp N.

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/bscb.19870960904/fullpdf

Reference28 articles.

1. Functionalization of Isophorone Involving Polychlorination. Part I: Heptachlorination Catalyzed by Dimethylformamide Hydrochloride and Solvolysis Induced by Concentrated Sulfuric Acid

2. 2 2 M. F. Grenier-Loustalot P. Iratcabal F. Métras J. Pétrissans Synthesis 33 1976 2 2 2 2

3. Hypochlorous acid. Reaction with conjugated ketones a synthesis of α-chloro-β,γ-unsaturated ketones

4. An unusually stable salt from isophorone and hydrogen bromide

5. D. B. Bright W. V. Furner E. R. White 1968

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4. Ionic Liquid as Reagent. A Green Procedure for the Regioselective Conversion of Epoxides to Vicinal-Halohydrins Using [AcMIm]X under Catalyst- and Solvent-Free Conditions;The Journal of Organic Chemistry;2005-04-12