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Differential analysis of aroma fingerprints of roasted pork from different breeds: A complementary approach using GC-IMS, GC-O-MS, and GC×GC-MS. [PDF]
Food Chem XZhang X +10 more
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Formation Mechanisms and Kinetic Modeling of Key Aroma Compounds During Qidan Tea Roasting. [PDF]
FoodsGao X, Wang S, Wang Y, Song H.
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Maillard Reaction-Derived Carbon Nanodots: Food-Origin Nanomaterials with Emerging Functional and Biomedical Potential. [PDF]
PharmaceuticsTörős G, Prokisch J.
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Proceedings of the Royal Society of London. Series B: Biological Sciences, 1990
Of the various types of alerting signals found in nature, odours are the least well understood. The worldwide distribution of pyrazines in plants, insects, terrestrial vertebrates, marine organisms, fungi and bacteria suggests that they are of special significance.
A, Woolfson, M, Rothschild
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Of the various types of alerting signals found in nature, odours are the least well understood. The worldwide distribution of pyrazines in plants, insects, terrestrial vertebrates, marine organisms, fungi and bacteria suggests that they are of special significance.
A, Woolfson, M, Rothschild
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2,3,5,6-Tetrakis(phenoxymethyl)pyrazine and 2,3,5,6-tetrakis(phenylsulfanylmethyl)pyrazine
Acta Crystallographica Section C Crystal Structure Communications, 2007The title compounds, C(32)H(28)N(2)O(4), (I), and C(32)H(28)N(2)S(4), (II), respectively, are tetrasubstituted pyrazines and both possess C(i) symmetry. They differ only in the hetero atom (X) of the -CH(2)XPh side-arm substituents: X = O in (I) and S in (II).
Tokouré, Assoumatine +2 more
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On the pyrazine and pyrazine–pyrimidine dimers
The Journal of Chemical Physics, 1986Spectra of the pyrazine-d4, pyrazine-h4–pyrazine-d4, and pyrazine-d4–pyrimidine dimer are obtained and analyzed with the help of Lennard-Jones–hydrogen-bonding (LJ–HB) potential energy calculations. The pyrazine isotopic hetero and homo dimers possess nearly identical spectra with the exception that the perpendicular dimer features are displaced to the
J. Wanna, E. R. Bernstein
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Pyrazine Analogues of Dipyrrolylquinoxalines
Organic Letters, 2003[structure: see text]. The synthesis of novel pyrazine derivatives bearing pyrrolic substituents is reported; the ability of these systems to bind certain biologically relevant anions in dichloromethane is also detailed.
Jonathan L, Sessler +3 more
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Vibrational spectra of [1H4]pyrazine and [2H4]pyrazine
Journal of the Chemical Society, Faraday Transactions 2, 1985Infrared and Raman spectra of [1H4]pyrazine and [2H4]pyrazine have been reinvestigated and a general assignment of all the observed bands is proposed which modifies some previous assignments of fundamental vibrations. The present assignment satisfies the isotopic product rule for i.r.- and Raman-active fundamentals.
Juan F. Arenas +4 more
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