Published November 10, 1987 | Version v1
Journal article

Synthesis of 4-methyl-8-oxo-4e-nonenal by the oxidative cleavage of e-geranylacetone. A 13C NMR spectral study of the intermediates

  • 1. Ukrainian Printing Industry Research Institute, Lvov (USSR)

Description

The oxidative cleavage of E-geranylacetone for the preparation of 4-methyl-8-oxo-4E-nonenal was improved. A 13C NMR spectral study of the intermediates, 9-bromo-6,10-dimethyl-10-hydroxy-5E-undecen-2-one, 6,10-dimethyl-9,10-epoxy-5E-undecen-2-one, and 6,10-dimethyl-9,10-dihydroxy-5E-undecen-2-one and a side-product, 2,2,5,5-tetramethyl-4-(3-methyl-7-oxo-3E-octenyl)-1,3-dioxolane showed the predominant conformations of these compounds in the solvents studied

Additional details

Publishing Information

Journal Title
J. Org. Chem. USSR (Engl. Transl.)
Journal Volume
23
Journal Issue
6
Series
J. Org. Chem. USSR (Engl. Transl.).
Journal Page Range
1093-1197
ISSN
0022-3271
CODEN
JOCYA

Optional Information

Notes
Translated from Zh. Org. Khim.; 23: No. 6, 1209-1215(Jun 1987).