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Enhanced mismatch negativity in harmonic compared with inharmonic sounds

Autor: Peter Vuust, Barbara Tillmann, Anne Caclin, Krzysztof Basiński, Lesly Fornoni, Elvira Brattico, Fanny Cholvy, J. Nasielski, D. R. Quiroga-Martinez

Publikováno v: Quiroga-Martinez, D R, Basiński, K, Nasielski, J, Tillmann, B, Brattico, E, Cholvy, F, Fornoni, L, Vuust, P & Caclin, A 2022, ' Enhanced mismatch negativity in harmonic compared with inharmonic sounds ', European Journal of Neuroscience, vol. 56, no. 5, pp. 4583-4599 . https://doi.org/10.1111/ejn.15769
European Journal of Neuroscience
European Journal of Neuroscience, 2022, ⟨10.1111/ejn.15769⟩

Many natural sounds have frequency spectra composed of integer multiples of a fundamental frequency. This property, known as harmonicity, plays an important role in auditory information processing. However, the extent to which harmonicity influences

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fe54b93f776a11c365fa6903494515f
https://pure.au.dk/ws/files/330386359/Eur_J_of_Neuroscience_2022_Quiroga_Martinez_Enhanced_mismatch_negativity_in_harmonic_compared_with_inharmonic_sounds.pdf

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Author response for 'Enhanced mismatch negativity in harmonic compared to inharmonic sounds'

Autor: null D. R. Quiroga‐Martinez, null K. Basiński, null J. Nasielski, null B. Tillmann, null E. Brattico, null F. Cholvy, null L. Fornoni, null P. Vuust, null A. Caclin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e7ec43f789a0176d3bd093352ee952c3
https://doi.org/10.1111/ejn.15769/v2/response1

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Chemoselectivity Reversals in Quinoxalines: The Reaction of 5-Chloro-6-Nitroquinoxaline with Nucleophiles

Autor: Cécile Moucheron, R. Nasielski-Hinkens, J. Nasielski

Publikováno v: Bulletin des Sociétés Chimiques Belges. 101:491-496

5‐Chloro‐6‐nitroquinoxaline 2, made in six steps from 2,3‐dichloronitro‐benzene, reacts 1) with piperidine to give 6‐nitro‐5‐piperidinoquinoxaline as the only product; 2) with methoxide to give a 95:5 ratio of 5‐methoxy‐6‐nitro�

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::34841be2031f450ef4150156479aee8a
https://doi.org/10.1002/bscb.19921010608

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Nucleophilic substitutions on 2-Chloro-3-Nitroquinoxaline

Autor: J. Nasielski, M. Loos, D. Grandjean, R. Nasielski-Hinkens, M. Kaisin

Publikováno v: Bulletin des Sociétés Chimiques Belges. 97:919-926

Piperidine, cyclohexylamine, methoxide ion and para‐thiocresolate ion react with 2‐chloro‐3‐nitroquinoxaline 1 by selectively substituting the nitro group, in contrast to the behavior of most ortho‐chloronitroaromatics which loose halide wh

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3699290d306951dc280a98b2be820bc6
https://doi.org/10.1002/bscb.19880971116

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Regioselectivity in the Reaction of Nitroquinoxaline-N-Oxides With Phosphoryl Chloride

Autor: R. Nasielski-Hinkens, J. Nasielski, E. Vande Vyver

Publikováno v: Bulletin des Sociétés Chimiques Belges. 95:663-670

6‐nitro‐, 2‐methyl‐6‐nitro‐ and 2,3‐dimethyl‐6‐nitroquinoxaline have been transformed into their N‐oxides by MCPBA in chloroform; the nitro group orients the oxygen atom preferentially to nitrogen atom N1, but the N4:N1 selectivit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1dab39ee8ff1fa43c75d07cc48eff1a3
https://doi.org/10.1002/bscb.19860950810

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Podands Based on 1,4,5,8-Tetra-Azaphenanthrene and Their Complexation With Ru2+

Autor: R. Nasielski‐Hinkens, S.‐H. Chao, J. Nasielski

Publikováno v: Bulletin des Sociétés Chimiques Belges. 98:375-386

Summary. New podands, based on 1,4,5,8‐tetra‐azaphenanthrene, have been synthesized from 2‐chloro‐1,4,5,8‐tetra‐azaphenanthrene 3; when the anchoring group is a nitrogen atom, the corresponding podands are, however, unstable. When reacted

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4cf3d03b80b305d7d65ffc08e0104fa4
https://doi.org/10.1002/bscb.19890980605

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A liposoluble cationic complex of Ru(II) based on 1,4,5,8-tetra-azaphenanthrene

Autor: M. ‐L. Garcia Y Abeledo, R. Nasielski-Hinkens, J. Nasielski

Publikováno v: Bulletin des Sociétés Chimiques Belges. 97:743-750

Reacting 2,2-dichlorododecanal with 1,2-diamino-4-nitrobenzene in dioxane in the presence of a base gives a 46% yield of 2-decyl-6-nitroquinoxaline, which after amination by hydroxylamine and reduction gave 5,6-diamino-2-decylquinoxaline. This diamin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2234caaca8fce4be89c95f5b41e1b96e
https://doi.org/10.1002/bscb.19880971003

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