Biotransformation of 1-acetoxy-p-menth-4(8)-ene with a suspension of cultured cells of Nicotiana tabacum
- 1 January 1983
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 10,p. 2475-2478
- https://doi.org/10.1039/p19830002475
Abstract
The biotransformation of 1-acetoxy-p-menth-4(8)-ene with a suspension of cultured cells of Nicotiana tabacum was investigated. It was found that the cultured cells had the ability to hydroxylate stereoselectively the exocyclic double bond from the side opposite to the acetoxy group and regioselectively the allylic position of the exocyclic double bond.This publication has 2 references indexed in Scilit:
- Stereoselectivity of the reduction of carvone and dihydrocarvone by suspension cells of Nicotiana tabacumPhytochemistry, 1982
- A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue CulturesPhysiologia Plantarum, 1962