Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jan Henrik, Halz"'
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 79, Iss 8, Pp 707-713 (2023)
Treatment of 3-formylacetylacetone with the amines benzylamine, tert-butylamine and (S)-methylbenzylamine led to the formation of the corresponding Schiff bases 3-[(benzylamino)methylidene]pentane-2,4-dione, C13H15NO2 (1), 3-[(tert-butylamino)methyli
Externí odkaz:
https://doaj.org/article/7aee4dbe3cef4acfb0aceef1ebb4b297
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 78, Iss 1, Pp 54-59 (2022)
Treatment of 3-formylacetylacetone with the isomeric o-, m- and p-aminobenzoic acids led to the formation of the corresponding Schiff bases, namely, 3-[(2-carboxyphenylamino)methylidene]pentane-2,4-dione, 1, 3-[(3-carboxyphenylamino)methylidene]penta
Externí odkaz:
https://doaj.org/article/9c16a5039d8e4ae78dd1928895200b79
Publikováno v:
IUCrData, Vol 7, Iss 11, p x221035 (2022)
The title complex, [Mg(C5H7O2)2(C6H16N2)], has been synthesized from magnesium acetylacetonate [Mg(acac)2] and tetramethylethylenediamine (TMEDA) in n-hexane. The monomeric complex consists of a central magnesium(II) atom, which is surrounded nearly
Externí odkaz:
https://doaj.org/article/a87c98adb55a47e280add10438bdd4ef
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 76, Iss 1, Pp 66-71 (2020)
The complexes bis(acetylacetonato-κ2O,O′)(N,N,N′,N′-tetramethylethylenediamine-κ2N,N′)manganese(II), [Mn(C5H7O2)2(C6H16N2)], bis(acetylacetonato-κ2O,O′)(N,N,N′,N′-tetramethylethylenediamine-κ2N,N′)iron(II), [Fe(C5H7O2)2(C6H16N2)],
Externí odkaz:
https://doaj.org/article/d402bb532dea4a06aea0565034ae2c7e
Autor:
René Csuk, Jan Henrik Halz, Sophie Hoenke, Markus Lang, Adrian Richter, Philipp Schulze, Lea Mann, Rüdiger W. Seidel
Publikováno v:
Amino Acids
Nα-2-thiophenoyl-d-phenylalanine-2-morpholinoanilide (MMV688845, IUPAC: N-(1-((2-morpholinophenyl)amino)-1-oxo-3-phenylpropan-2-yl)thiophene-2-carboxamide) from the Pathogen Box® library (Medicines for Malaria Ventures, MMV) is a promising lead com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b60e9a0372e6fc6f703ec7f9a238e9ff
http://europepmc.org/articles/PMC8325651
http://europepmc.org/articles/PMC8325651
Publikováno v:
Zeitschrift für anorganische und allgemeine Chemie. 647:922-930
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b080d732bfabd1df91264aa061a7513
https://doi.org/10.1002/zaac.202000436
https://doi.org/10.1002/zaac.202000436
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications
The condensation products of the o-, m- and p- isomers of aminobenzoic acid and 3-formylaceylacetone were synthesized and structurally characterized. As a result of the different substitution patterns, their crystal structures are governed by dif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::22537e912f05bd45b1e3c44cfa6e169f
https://pubmed.ncbi.nlm.nih.gov/35079425
https://pubmed.ncbi.nlm.nih.gov/35079425
Publikováno v:
Journal of Molecular Structure. 1251:132033
Azelastine is among the most frequently used drugs; however, knowledge and solid data about its metabolites are scarcely found in literature. Thus, microsomal oxidation of azelastine is thought to produce the corresponding N-oxides, However, until no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6066b3c547f66a254857905632a51d1f
https://doi.org/10.1016/j.molstruc.2021.132033
https://doi.org/10.1016/j.molstruc.2021.132033
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications
Syntheses and crystal structures of three metal complexes [M(acac)2(TMEDA)] [M = Mn (1), Fe (2) and Zn (3)] with acetylacetonate and N,N,N′,N′-tetramethylethylenediamine are discussed.
The complexes bis(acetylacetonato-κ2 O,O′
The complexes bis(acetylacetonato-κ2 O,O′
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3eddcfa3ac8540f35851c84c5609892e
https://pubmed.ncbi.nlm.nih.gov/31921454
https://pubmed.ncbi.nlm.nih.gov/31921454