Oxidation-reduction relationship between cycloalkanones and the corresponding cycloalkanols in a cell suspension culture of Nicotiana tabacum
- 1 April 1983
- journal article
- research article
- Published by Springer Nature in Plant Cell Reports
- Vol. 2 (2) , 66-68
- https://doi.org/10.1007/bf00270167
Abstract
The interconversion between 5 to 8-membered cycloalkanones and the corresponding cycloalkanols by a cell suspension culture of Nicotiana tabacum was studied. It was found that the interconversion is at equilibrium and the balance in the equilibrium depends on the number of carbon atoms in the carbocyclic ring of the substrates; the equilibrium in the interconversion of the 6-membered compound lies toward the side of the cycloalkanol, while in the cases of the 5, 7, and 8-membered compounds the cycloalkanones are favoured.Keywords
This publication has 6 references indexed in Scilit:
- THE STEREOSPECIFIC HYDROXYLATION OF ENDOCYCLIC ETHYLENIC LINKAGE IN THE BIOTRANSFORMATION OF α-TERPINYL ACETATE WITH CULTURED SUSPENSION CELLS OF NICOTIANA TABACUMChemistry Letters, 1982
- Stereoselectivity of the reduction of carvone and dihydrocarvone by suspension cells of Nicotiana tabacumPhytochemistry, 1982
- The Biotransformation of Foreign Substrates by Tissue Cultures. I. The Hydroxylation of Linalool and Its Related Compounds with the Suspension Cells of Nicotiana tabacumBulletin of the Chemical Society of Japan, 1981
- Enzymes in organic syntheses. 19. Evaluation of the stereoselectivities of horse liver alcohol dehydrogenase; catalyzed oxidoreductions of hydroxy- and ketothiolanes, -thianes, and -thiepanesCanadian Journal of Chemistry, 1981
- BIOTRANSFORMATION OF FOREIGN SUBSTRATES WITH CALLUS TISSUES. TRANSFORMATION OF TERPINEOLS WITH TOBACCO SUSPENSION CELLSChemistry Letters, 1980
- BIOTRANSFORMATION OF MONOTERPENES BY TOBACCO TISSUE CULTURES. SELECTIVE HYDROXYLATION OF TRANS-METHYL GROUP IN ISOPROPYRIDENE GROUPChemistry Letters, 1976