Microbiological transformations. 24. Synthesis of chiral building blocks via stereoselective dihydroxylation of citronellol enantiomers
- 30 November 1992
- journal article
- research article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 3 (11) , 1373-1376
- https://doi.org/10.1016/0957-4166(92)80009-l
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Microbiological Transformations. 21. An expedient route to both enantiomers of Marmin and Epoxyauraptens via microbiological dihydroxylation of 7-geranyloxycoumarinTetrahedron: Asymmetry, 1991
- Microbial transformationsd. 19. Asymmetric dihydroxylation of the remote double bond of geraniol: a unique stereochemical control allowing easy access to both enantiomers of geraniol-6,7-diolThe Journal of Organic Chemistry, 1991
- Microbial transformations. 12. Regiospecific and asymmetric oxidation of the remote double bond of geraniolThe Journal of Organic Chemistry, 1989
- Syntheses en serie racemique et en serie optiquement active d'une famille de derives oxygenes naturels de l'ombelliferone. Structure spatiale du (-)epoxy-3'6' aurapteneTetrahedron, 1988
- Organoboron compounds in organic synthesis. 2. Asymmetric reduction of dialkyl ketones with (R,R)- or (S,S)-2,5-dimethylborolaneJournal of the American Chemical Society, 1986
- Synthesis of the optical isomers of 3-methyl-6-isopropenyl-9-decen-1-yl acetate, a component of the California red scale pheromoneThe Journal of Organic Chemistry, 1980
- Sex pheromone of the California red scale, Aonidiella aurantiiNature, 1977
- Synthetic studies on optically active epoxyterpenes from L-glutamic acid-I syntheses of R-(+)-epoxygeraniol, R-(+)-marmin and R-(+)-epoxyauraptenTetrahedron Letters, 1976