Zobrazeno 1 - 10
of 301
pro vyhledávání: '"J.‐C. Halle"'
Autor:
Szőnyi, Ádám1 (AUTHOR) szonyi.adam@stud.semmelweis.hu, Nyárády, Balázs Bence1 (AUTHOR), Philippovich, Márton1 (AUTHOR), Dobai, Adrienn2 (AUTHOR), Sari, Ekrem Anil3 (AUTHOR) ekremanil.sari@deu.edu.tr, Szőnyi, András4 (AUTHOR), Nagy, Anikó Ilona1 (AUTHOR), Dósa, Edit1 (AUTHOR) dosa.edit@semmelweis.hu
Publikováno v:
Life (2075-1729). Nov2024, Vol. 14 Issue 11, p1440. 13p.
Publikováno v:
Journal of Fluorine Chemistry. 107:387-395
The enzymatic effect of locust tissues upon hydrolysis of the fluorinated Δ 2 -oxazoline-1,3 Ia was elucidated using 19 F[ 1 H] NMR monitoring. In a phosphate buffer at pH=7.4 (mean physiological pH of locust tissues), the substrate Ia hydrolyses sl
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2001, 42 (27), pp.4499-4501. ⟨10.1016/S0040-4039(01)00774-2⟩
Tetrahedron Letters, Elsevier, 2001, 42 (27), pp.4499-4501. ⟨10.1016/S0040-4039(01)00774-2⟩
International audience; Treatment of 4,6-dinitrobenzofuroxan (DNBF) with the imidazoline 1-NRf is found to afford a zwitterionic nitrogen-bonded complex (2-NRf±) which, in the presence of base (Et3N), undergoes a slow but quantitative transformation
Publikováno v:
ChemInform. 23
Publikováno v:
ChemInform. 23
Publikováno v:
ChemInform. 29
Publikováno v:
Organicbiomolecular chemistry. 1(10)
Nucleophilic substitutions of 4-chloro-7-nitrobenzofurazan (NBD-Cl) and 3-methyl-1-(4-nitrobenzofurazanyl)-imidazolium ions (NBD-Im+) with a series of 4-X-substituted anilines have been kinetically investigated in 70-30 (v/v) and 20-80 (v/v) H2O-Me2S
Publikováno v:
The Journal of organic chemistry. 62(21)
The reaction of ethyl vinyl ether (2 equiv) with 4,6-dinitrobenzofuroxan (DNBF, 1 equiv) in dichloromethane affords a mixture of two diastereomeric dihydrooxazine N-oxide adducts, 5a and 5b, in a 4:1 ratio. Further addition of the enol reagent to thi
Autor:
Muriel Sebban, Gilles Moutiers, J.‐C. Halle, Régis Goumont, François Terrier, I. Cangelosi, Erwin Buncel
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2000, 65 (22), pp.7391-7398. ⟨10.1021/jo0005114⟩
Journal of Organic Chemistry, 2000, 65 (22), pp.7391-7398. ⟨10.1021/jo0005114⟩
Journal of Organic Chemistry, American Chemical Society, 2000, 65 (22), pp.7391-7398. ⟨10.1021/jo0005114⟩
Journal of Organic Chemistry, 2000, 65 (22), pp.7391-7398. ⟨10.1021/jo0005114⟩
In investigating the reactivities of aza analogues of super-electrophile 4,6-dinitrobenzofuroxan (DNBF, 1), we have found that the nitro-substituted pyridofuroxan 2 gives a remarkably stable hydrate 3 in aqueous solution (as evidenced by the requirem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34eb51ceb9259539bcac4f8d75ebe2e1
https://hal-normandie-univ.archives-ouvertes.fr/hal-02546273
https://hal-normandie-univ.archives-ouvertes.fr/hal-02546273
Autor:
Deshayes, Samuel1,2 (AUTHOR) samuel.deshayes@gmail.com, Baugé, Caroline2 (AUTHOR), Dupont, Pierre-Antoine2 (AUTHOR), Simard, Christophe2 (AUTHOR), Rida, Hanan2 (AUTHOR), de Boysson, Hubert1,2 (AUTHOR), Manrique, Alain2,3 (AUTHOR), Aouba, Achille1,2 (AUTHOR) aouba-a@chu-caen.fr
Publikováno v:
EJNMMI Research. 11/29/2023, Vol. 13 Issue 1, p1-9. 9p.