Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Gordon M. Elsey"'
Autor:
Dennis K. Taylor, Gordon M. Elsey, Heike Ebendorff-Heidepriem, George K. Skouroumounis, Mai-Chi Nguyen, Tanya M. Monro, Rachel L. Moore
Publikováno v:
Sensors, Vol 12, Iss 8, Pp 10759-10773 (2012)
Sulfur dioxide (SO2) is important in the winemaking process as it aids in preventing microbial growth and the oxidation of wine. These processes and others consume the SO2 over time, resulting in wines with little SO2 protection. Furthermore, SO2 and
Externí odkaz:
https://doaj.org/article/b2e3db10885c40d0b5968fda6d1c4287
Autor:
Heike Ebendorff-Heidepriem, Rachel L. Moore, Tanya M. Monro, M. Nguyen, George K. Skouroumounis, Gordon M. Elsey, Dennis K. Taylor
Publikováno v:
Sensors; Volume 12; Issue 8; Pages: 10759-10773
Sensors (Basel, Switzerland)
Sensors, Vol 12, Iss 8, Pp 10759-10773 (2012)
Sensors (Basel, Switzerland)
Sensors, Vol 12, Iss 8, Pp 10759-10773 (2012)
Sulfur dioxide (SO2) is important in the winemaking process as it aids in preventing microbial growth and the oxidation of wine. These processes and others consume the SO2 over time, resulting in wines with little SO2 protection. Furthermore, SO2 and
Autor:
Mark A. Sefton, Natoiya D. R. Lloyd, George K. Skouroumounis, Dimitra L. Capone, Gordon M. Elsey, Maurizio Ugliano, Dennis K. Taylor
Publikováno v:
Journal of Agricultural and Food Chemistry. 59:1338-1343
The fermentations, at a commercial winery, of six different grape musts encompassing the varieties Riesling, Chardonnay, Sauvignon blanc, Shiraz, Grenache, and Pinot noir were monitored for damascenone concentration. In every case, the concentration
Autor:
Mark A. Sefton, Katryna A. van Leeuwen, David W. Jeffery, Dennis K. Taylor, Kevin H. Pardon, Gordon M. Elsey, Dimitra L. Capone
Publikováno v:
Journal of Agricultural and Food Chemistry. 59:953-959
A new method has been developed for the quantitation of 1,8-cineole in red and white wines using headspace solid-phase microextraction (SPME) combined with stable isotope dilution analysis (SIDA) and gas chromatography-mass spectrometry (GC-MS). An e
Autor:
Kevin H. Pardon, Adrian D. Coulter, Merran A. Daniel, Dimitra L. Capone, Mark A. Sefton, K.A. van Leeuwen, Gordon M. Elsey
Publikováno v:
Australian Journal of Grape and Wine Research. 16:210-217
Background and Aims: The aim of this study was to determine the cause of taints and off-flavours in a number of commercial wines and to develop methods for quantitative analysis of the compounds responsible. Methods and Results: Three compounds, 2-ch
Autor:
Mark A. Sefton, Gordon M. Elsey, Dimitra L. Capone, Rachel C. Cooke, Richard Gawel, Katryna A. van Leeuwen
Publikováno v:
Journal of Agricultural and Food Chemistry. 57:2462-2467
The individual enantiomers of gamma-octalactone (1), gamma-nonalactone (2), gamma-decalactone (3) and gamma-dodecalactone (4) have been synthesized. The (R) series of enantiomers was prepared from L-glutamic acid by a strategy involving deamination a
Publikováno v:
Australian Journal of Grape and Wine Research. 15:93-96
Background and Aims: Knowledge of the formation and fate of aroma compounds is important to an understanding of the processes that affect wine composition and flavour. This study aimed to investigate the competitive formation and degradation of 1,1,6
Publikováno v:
Journal of Agricultural and Food Chemistry. 57:991-995
The identification of 4-S-glutathionyl-4-methylpentan-2-one (glut-4-MMP) by high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) experiments in a Sauvignon Blanc juice extract is described. Synthesis of an authentic reference
Publikováno v:
Journal of Agricultural and Food Chemistry. 57:348-352
Stable isotope dilution assays have been developed for gamma-octalactone (1), gamma-nonalactone (2), gamma-decalactone (3) and gamma-dodecalactone (4) in both white and red wines for the first time. (2)H(7)-analogues of each lactone were prepared for
Publikováno v:
Journal of Agricultural and Food Chemistry. 56:9183-9189
Storage of megastigma-4,6,7-trien-3,9-diol (5), and megastigma-3,4-dien-7-yn-9-ol (6) in aqueous ethanol solution at pH 3.0 and 3.2 gave exclusively damascenone (1) and damascenone adducts at room temperature. The diol (5) had half-lives for the conv