The microbial transformations of 2,6-and 3,5-dimethylcyclohexanone were investigated using the plant pathogenic fungus, Glomerella cingulata. With this organism 2,6-and 3,5dimethylcyclohexanone gave the corresponding 2,6-and 3,5-dimethylcyclohexanol. The metabolites from 2,6-dimethylcyclohexanone in
Mass spectrometric fragmentation of 2-isopropenyl-2,5-dimethylcyclohexanone and 2-isopropyl-2,5-dimethylcyclohexanone
β Scribed by Kulkarni, M. V.; Eisenbraun, E. J.; Hamming, M. C.
- Book ID
- 127015386
- Publisher
- American Chemical Society
- Year
- 1970
- Tongue
- English
- Weight
- 431 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
The detailed mass spectral fragmentation pathways of a series of both naturally occurring and synthetic %methyl-3alkyl-2-alkenylpyrazines have been elucidated with the aid of deuterium labels placed specifically in the alkenyl side-chain. The influence on the fragmentation pattern of the stereochemi