排序方式: 共有7条查询结果,搜索用时 15 毫秒
1
1.
Determination of the geographical origin of Brazilian wines by isotope and mineral analysis 总被引:1,自引:0,他引:1
Dutra SV Adami L Marcon AR Carnieli GJ Roani CA Spinelli FR Leonardelli S Ducatti C Moreira MZ Vanderlinde R 《Analytical and bioanalytical chemistry》2011,401(5):1575-1580
In the present research, we studied wines from three different south Brazilian winemaking regions with the purpose of differentiating
them by geographical origin of the grapes. Brazil's wide territory and climate diversity allow grape cultivation and winemaking
in many regions of different and unique characteristics. The wine grape cultivation for winemaking concentrates in the South
Region, mainly in the Serra Gaúcha, the mountain area of the state of Rio Grande do Sul, which is responsible for 90% of the
domestic wine production. However, in recent years, two new production regions have developed: the Campanha, the plains to
the south and the Serra do Sudeste, the hills to the southeast of the state. Analysis of isotopic ratios of 18O/16O of wine water, 13C/12C of ethanol, and of minerals were used to characterize wines from different regions. The isotope analysis of δ18O of wine water and minerals Mg and Rb were the most efficient to differentiate the regions. By using isotope and mineral
analysis, and discrimination analysis, it was possible to classify the wines from south Brazil. 相似文献
2.
Guanaes Lais Danciguer Guimarães Matheus Murmel Ducatti Diogo R. B. Duarte Maria Eugênia R. Barreira Sandra M. W. Noseda Miguel D. Gonçalves Alan Guilherme 《Chemistry of Heterocyclic Compounds》2021,57(12):1195-1203
Chemistry of Heterocyclic Compounds - In the present work, we have synthesized new molecular hybrids consisting of porphyrin ring system connected at the meso positions with phenyl groups and/or,... 相似文献
3.
Alan G. Gonçalves Diogo R. B. Ducatti T. Bruce Grindley M. Eugênia R. Duarte Miguel D. Noseda 《Journal of the American Society for Mass Spectrometry》2010,21(8):1404-1416
We have prepared a number of isomeric red seaweed galactan-derivative sulfated oligosaccharides to determine whether there
were diagnostic differences among the isomeric mass spectra obtained using ESI CID MS/MS (triple quadrupole instrument). Fragmentation
of the single or multicharged molecular ions from di-, tetra-, and hexasaccharides indicated that the relative positioning
of the sulfate groups and type of monosaccharide unit affect the rate of cleavage of the glycosidic bonds. We also performed
a comparative [M-Na]− fragmentation study of positional isomers of sulfated disaccharides that present all four monosulfation possibilities on
the galactopyranosidic ring. In this case, negative-ion ESI CID MS/MS approach gave diagnostic product ions from cross-ring
cleavages along with the same main B1 ion (from sulfated Galp), at m/z 241, for all isomers. The isomeric disaccharides were also submitted to increased spray energy conditions inducing in-source
fragmentation; preformed B1 ions were then fragmented to give similar product ions as those found in [M-Na]− analysis. Evaluation of the relative abundances mainly for cross-ring fragment ions at m/z 138, 139, 151, 153 allowed clear distinction among the members of the disaccharide series. The different ratios for m/z 151/153 ions were consistent with the predominance of m/z 153 being related to the cases when the bond involved in the cleavage process links a sulfated carbon. A quadrupole ion trap
instrument (MSn analysis) was also utilized to compare the results obtained with the triple quadrupole instrument. 相似文献
4.
Stephanie M.S. LóDiogo R.B. Ducatti M. Eugênia R. DuarteSandra M.W. Barreira Miguel D. NosedaAlan G. Gonçalves 《Tetrahedron letters》2011,52(13):1441-1443
The oxidative step of the two-step, one-flask synthesis of meso-tetraarylporphyrins is herein conducted with heterogeneous oxidant SeO2 instead of the usual quinones DDQ or p-chloranil. Evaluation of BF3O(Et)2 or I2 amount for the condensation of the first step combined with the excess of SeO2 defined porphyrin synthesis conditions employing benzaldehydes and pyrrole (or 5-phenyldipyrromethane) as starting materials. The simplicity of the workup, allied with reaction mild conditions, makes this method a good option for the synthesis of this kind of compound. 相似文献
5.
Ingrid F. Zattoni Lais D. Guanaes Letícia B. Cerqueira Roberto Pontarolo Diogo R.B. Ducatti M. Eugênia R. Duarte Miguel D. Noseda Angela C.L.B. Trindade Alan G. Gonçalves 《Tetrahedron letters》2019,60(40):151129
We have evaluated four 1,4-dihydropyridines (DHPs 1a, 1b, 1c and 1d) as reducing agents, which presented free (hydrogenated) or phenyl-substituted N-1 and C-4 positions of the DHP ring. Reactions combining each of the DHP and different amounts of BF3OEt2 were evaluated for the reduction of imine 2a (N-benzylideneaniline). DHP simultaneously substituted at N-1 and C-4 (1a), and DHP substituted at C-4 (1b) gave lower yields for reduction of 2a in comparison with DHPs 1c and 1d (both unsubstituted at the C-4 position). By evaluating the amount of added BF3OEt2 to the reaction mixture, we have found that DHP 1c (substituted at N-1) provided its best yield for amine 3a (82%) when associated with stoichiometric amounts BF3OEt2, while DHP 1d (N-1- and C-4-unsubstituted derivative) was more effective (90% yield) with catalytic quantities of the Lewis acid. The reaction system using DHP 1c under stoichiometric BF3OEt2 could also be successfully applied with additional imine examples and under reductive amination conditions. 相似文献
6.
Carneiro Jaqueline Dallagnol Juliana C. C. Veiga Andressa Noseda Miguel D. Duarte Maria Eugnia R. Filho Marco A. Carvalho Ducatti Diogo R. B. Gonalves Alan G. Murakami Fbio S. 《Journal of Thermal Analysis and Calorimetry》2022,147(12):6755-6764
Journal of Thermal Analysis and Calorimetry - Porphyrins have exquisite photophysical and electronic properties that enable their use in photodynamic therapy. Even though the thermodynamic behavior... 相似文献
7.
1