Výsledky vyhledávání - "Sebastian Saloman"

Electronic Tuneable Dynamic and Electrochemical Behavior ofN-(Diferrocenylmethylene)anilines

Autor: Heinrich Lang, Sebastian Saloman, Marcus Korb, Manuel Schwind, Alexander Hildebrandt

Publikováno v: Zeitschrift für anorganische und allgemeine Chemie. 641:2282-2290

N-(Diferrocenylmethylene)anilines Fc2C=N-4-C6H4–R [3a R = CF3; 3b R = Cl; 3c R = H; 3d R = CH3; 3e R = OCH3; Fc = Fe(η5-C5H4)(η5-C5H5)] with different electron-donating or -withdrawing functionalities were synthesized by a Schiff base reaction of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ca8edaefcbc955e704c63a03e940d9b1
https://doi.org/10.1002/zaac.201500557

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Can Silicon Make an Excellent Drug Even Better? An in vitro and in vivo Head-to-Head Comparison between Loperamide and Its Silicon Analogue Sila-Loperamide

Autor: Duncan Armstrong, Eric Wellner, Marcel Geyer, Sebastian Saloman, Reinhold Tacke, Ulrik Jurva

Publikováno v: ChemMedChem. 10:911-924

Loperamide (1a), an opioid receptor agonist, is in clinical use as an antidiarrheal agent. Carbon/silicon exchange (sila-substitution) at the 4-position of the piperidine ring of 1a (R3 COH→R3 SiOH) leads to sila-loperamide (1b). Sila-loperamide wa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c688d0be65bcb97e7ff655ea114bf94f
https://doi.org/10.1002/cmdc.201500040

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1, 1'-Bis(thymine)ferrocene Nucleoside : Synthesis and Study of Its Stereoselective Formation

Autor: Iurii Anisimov, Krzysztof Woźniak, Heinrich Lang, Davor Šakić, Alexander Hildebrandt, Sebastian Saloman, Konrad Kowalski, Valerije Vrček, Damian Trzybiński

The synthesis of 1,1'-bis(thymine)ferrocene nucleoside is reported. This nucleoside was obtained in a two-step synthetic methodology including a Michael addition reaction of 1,1'-bis(3-chloropropionyl)ferrocene with thymine to afford the bis(thymine)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78dcedb2068842c56e26b5c7d9e8720c
https://doi.org/10.1002/cplu.201700215

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Cymantrene, Cyrhetrene and Ferrocene Nucleobase Conjugates: Synthesis, Structure, Computational Study, Electrochemistry and Antitrypanosomal Activity

Autor: Valerije Vrček, Dietmar Steverding, Heinrich Lang, Alexander Hildebrandt, Artur Jabłoński, Konrad Kowalski, Agnieszka J. Rybarczyk-Pirek, Łukasz Szczupak, Sebastian Saloman

Publikováno v: ChemPlusChem. 82(2)

A series of 11 cymantrene and cyrhetrene nucleobase conjugates, together with the hitherto unreported N7 isomer of a ferrocene–adenine conjugate were synthesised and characterised. The synthetic approach involved a Michael addition reaction of in-s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fb4c07ab2fc1e956fb79918a5015685
https://pubmed.ncbi.nlm.nih.gov/31961557

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