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pro vyhledávání: '"Michal, Kriegelstein"'
Autor:
Michal Kriegelstein, Aleš Marek
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 65:244-253
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 64:500-512
Convenient and straightforward synthesis of ibrutinib labeled by carbon-13 isotope is reported. Isotopically labeled building block is introduced in the last step of reaction sequence affording sufficient isolated yield (7%) of [13 C6 ]-ibrutinib cal
Autor:
Michal, Kriegelstein, Aleš, Marek
Publikováno v:
Journal of labelled compoundsradiopharmaceuticalsREFERENCES. 65(9)
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Publikováno v:
The Journal of Organic Chemistry. 85:12912-12921
Axially chiral trifluoromethylbenzimidazolylbenzoic acid (TBBA) was used as a chiral derivatization agent for the assignment of the absolute configuration of β-chiral primary alcohols. The structures varied from simple aliphatic alcohols to complex
Publikováno v:
Journal of labelled compoundsradiopharmaceuticalsREFERENCES. 64(13)
Convenient and straightforward synthesis of ibrutinib labeled by carbon-13 isotope is reported. Isotopically labeled building block is introduced in the last step of reaction sequence affording sufficient isolated yield (7%) of [
Publikováno v:
Journal of pharmaceutical and biomedical analysis. 206
At present, therapeutic drug monitoring is the standard in pharmacotherapy using medications with a narrow therapeutic index or showing serious adverse effects, such as in the case of ibrutinib. A technique commonly used for this purpose is liquid ch
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 206:114366
At present, therapeutic drug monitoring is the standard in pharmacotherapy using medications with a narrow therapeutic index or showing serious adverse effects, such as in the case of ibrutinib. A technique commonly used for this purpose is liquid ch
Autor:
Sandra Benická, Michal Kriegelstein, Adam Přibylka, Antonín Lyčka, David Profous, Tereza Volná, Zdeněk Trávníček, Petr Cankař
Publikováno v:
The Journal of organic chemistry. 84(18)
Racemic 2-(2-trifluoromethyl)-1H-benzo[d]imidazol-1-yl)benzoic acid (TBBA) was synthesized in three steps from 1-fluoro-2-nitrobenzene. Target (P)- and (M)-TBBA atropisomers were stable with a racemization barrier above 30 kcal/mol. As a chiral deriv