Hydroxylation of menthols and cineoles withm-chloroperbenzoic acid
- 1 February 1986
- journal article
- research article
- Published by Springer Nature in Cellular and Molecular Life Sciences
- Vol. 42 (2), 201-203
- https://doi.org/10.1007/bf01952469
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Allelopathic substances, (.+-.)-p-menthane-3,8-diols isolated from eucalyptus citriodora hook.Agricultural and Biological Chemistry, 1982
- Eucalyptus as biomass. Novel compounds from microbial conversion of 1,8-cineole.Agricultural and Biological Chemistry, 1982
- Regio‐ and Stereospecific Hydroxylation of Alicyclic Hydrocarbons with Substituted Perbenzoic AcidsAngewandte Chemie International Edition in English, 1979
- Products of 1,8-Cineole Oxidation by a PseudomonadAustralian Journal of Chemistry, 1979
- Studies on the wild mints of Tokai districts. VI. Absolute configuration of (+)-1-acetoxy-p-menth-3-one isolated from essential oil of Mentha gentilis (L.).Agricultural and Biological Chemistry, 1975
- Functionalization of non-activated carbon atomsPublished by Walter de Gruyter GmbH ,1975
- Centenary Lecture. Biomimetic chemistryChemical Society Reviews, 1972
- Sesquiterpenes having a five-membered ether-ring in the moleculePublished by Walter de Gruyter GmbH ,1970
- Synthesis of Two Isomeric p-Menthane-3,4-diols and Their Pinacolic Dehydration to a Menthone Mixture1The Journal of Organic Chemistry, 1960