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The Oxidation of 1,8-Cineole by Pseudomonas flava

RM Carman, IC Macrae and MV Perkins
39(11) pp.1739 - 1746


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Biotransformation of 1,8-cineole in the brushtail possum (Trichosurus vulpecula)
Boyle R., McLean S., Davies N. W.
Xenobiotica. 2000 30(9). p.915
Enantiomer separation of 2‐halocarboxylic acid esters by chiral complexation gas chromatography
Schurig V., Ossig A., Link R.
Journal of High Resolution Chromatography. 1988 11(1). p.89
Biotechnology (1998)
Holland Herbert L.
Physiology of Biodegradative Microorganisms (1991)
Trudgill Peter W.
CYP101J2, CYP101J3, and CYP101J4, 1,8-Cineole-Hydroxylating Cytochrome P450 Monooxygenases from Sphingobium yanoikuyae Strain B2
Unterweger Birgit, Bulach Dieter M., Scoble Judith, Midgley David J., Greenfield Paul, Lyras Dena, Johanesen Priscilla, Dumsday Geoffrey J., Müller V.
Applied and Environmental Microbiology. 2016 82(22). p.6507
Microbial metabolism of monoterpenes ? recent developments
Trudgill Peter W.
Biodegradation. 1990 1(2-3). p.93
1,8‐Cineole: Chemical and Biological Oxidation Reactions and Products
Azerad Robert
ChemPlusChem. 2014 79(5). p.634
Metabolites of dietary 1,8-cineole in the male koala (Phascolarctos cinereus)
Boyle Rebecca, McLean Stuart, Foley William, Davies Noel W, Peacock Evan J, Moore Ben
Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology. 2001 129(4). p.385
Microbial monoterpene transformations—a review
Marmulla Robert, Harder Jens
Frontiers in Microbiology. 2014 5
Synthesis of the fragrance terpene epoxides and selective monocyclization promoted by camphor and oxone®
Gaikwad Ravindra D., Kabiraj Shilpi S., Bhat Sujata V.
Flavour and Fragrance Journal. 2016 31(5). p.350
Selective hydroxylation of 1,8- and 1,4-cineole using bacterial P450 variants
Lee Joel H.Z., Wong Siew Hoon, Stok Jeanette E., Bagster Sarah A., Beckett James, Clegg Jack K., Brock Aidan J., De Voss James J., Bell Stephen G.
Archives of Biochemistry and Biophysics. 2019 663 p.54
Synthesis and Antibacterial Activity of Highly Oxygenated 1,8-Cineole Derivatives
Villecco Margarita B., Catalán Julieta V., Vega Marta I., Garibotto Francisco M., Enriz Ricardo D., Catalán César A. N.
Natural Product Communications. 2008 3(3). p.1934578X0800300
Biotechnology Set (2001)
Holland Herbert L.
Stereospecific hydroxylation of 1,8-cineole using a microbial biocatalyst
Wei Guo Liu, Rosazza John P.N.
Tetrahedron Letters. 1990 31(20). p.2833
Two New Biocatalysts for Improved Biological Oxidation of 1,8-Cineole
Rasmussen Jo-Anne M., Henderson Kylie A., Straffon Melissa J., Dumsday Geoffrey J., Coulton Jacqueline, Zachariou Michael
Australian Journal of Chemistry. 2005 58(12). p.912
Identification of pheromone candidates for the eucalyptus weevil, Gonipterus platensis (Coleoptera, Curculionidae)
Branco Sofia, Mateus Eduardo Pires, Gomes da Silva Marco Diogo Richter, Mendes Davide, Pereira Maria Manuela Araújo, Schütz Stefan, Paiva Maria Rosa
Journal of Applied Entomology. 2020 144(1-2). p.41
Preparation and use of (S)-O-acetyllactyl chloride (Mosandl's reagent) as a chiral derivatizing agent
Buisson Didier, Azerad Robert
Tetrahedron: Asymmetry. 1999 10(15). p.2997
Biooxidation of 1,8-cineole by Aspergillus terreus
García Carlos, Rodríguez Paula, Días Eduardo, Heinzen Horacio, Menéndez Pilar
Journal of Molecular Catalysis B: Enzymatic. 2009 59(1-3). p.173
Metabolism of 1,8-cineole in tea tree (Melaleuca alternifolia andM. linariifolia) by pyrgo beetle (Paropsisterna tigrina)
Southwell Ian A., Maddox Craig D. A., Zalucki Myron P.
Journal of Chemical Ecology. 1995 21(4). p.439
Biochemistry of microbial degradation (1994)
Trudgill Peter W.
Photo-oxygenation of 1,8-cineole by molecular oxygen catalysed by (Bu4N)4W10O32
Zakrzewski J., Giannotti C.
Journal of Photochemistry and Photobiology A: Chemistry. 1992 63(2). p.173
Enantiomer analysis by complexation gas chromatography
Schurig V.
Journal of Chromatography A. 1988 441(1). p.135
Synthesis of oxygenated cineole derivatives from cineole: utility of cytochrome P450cin as an enantioselective catalyst
Farlow Anthony J., Bernhardt Paul V., De Voss James J.
Tetrahedron: Asymmetry. 2013 24(5-6). p.324
Preparation and Absolute Configuration of (1R,4R)-(+)-3-Oxo-, (1S,4S)-(-)-3-Oxo- and (1R,3S,4R)-(+)-3-Acetyloxy-5-oxo-1,8-cineole
Loandos María del H., Villecco Margarita B., Burgueño-Tapia Eleuterio, Joseph-Nathan Pedro, Catalán César A. N.
Natural Product Communications. 2009 4(11). p.1934578X0900401
Oxidation of natural compounds catalyzed by Mn(III) porphyrin complexes
Cavaleiro JoséA.S., Nascimento Graça M.S.F.C., Neves Maria G.P.M.S., Pinto Maria T., Silvestre Armando J.D., Vicente Maria G.H.
Tetrahedron Letters. 1996 37(11). p.1893
Thauera linaloolentis sp. nov. and Thauera terpenica sp. nov., Isolated on Oxygen-containing Monoterpenes (Linalool, Menthol, and Eucalyptol and Nitrate
Foss S., Harder J.
Systematic and Applied Microbiology. 1998 21(3). p.365
Chiral Separations (1988)
Schurig Volker, Link Rainer

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