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ChemInform Abstract: ORGANOMERCURY COMPOUNDS PART 21, BISTETRACHLORONITROPHENYLMERCURY COMPOUNDS
Chemischer Informationsdienst, 1975AbstractDie Titelverbindungen (III) werden durch Mercurierung entsprechender Tetrachlornitrobenzole (I) mit Hg(II)‐trifluoracetat (II) dargestellt.
GLEN B. DEACON +2 more
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Journal of Medicinal Chemistry, 1978
P,P-Bis(1-aziridinyl)-N-adamantylphosphinic amide and N,N'-bis(ethylene)-P-(1-adamantyl)phosphonic diamide were synthesized as potential anticancer and male antifertility agents. Log P values (octanol-water) of the agents were determined and compared to calculated values.
L A, Cates, M B, Cramer, L, Williams
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P,P-Bis(1-aziridinyl)-N-adamantylphosphinic amide and N,N'-bis(ethylene)-P-(1-adamantyl)phosphonic diamide were synthesized as potential anticancer and male antifertility agents. Log P values (octanol-water) of the agents were determined and compared to calculated values.
L A, Cates, M B, Cramer, L, Williams
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1975
Publisher Summary Carbonyl compounds are most often separated in their hydrogen sulfite form by ion-exchange chromatography on basic resins. The use of liquid chromatography for the systematic separation of free aldehydes and ketones is not extensive.
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Publisher Summary Carbonyl compounds are most often separated in their hydrogen sulfite form by ion-exchange chromatography on basic resins. The use of liquid chromatography for the systematic separation of free aldehydes and ketones is not extensive.
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Compound 21 Prevents Salt Induced Myocardial Hypertrophy
The FASEB Journal, 2016Objective To evaluate the role of Compound 21 (C21) in a model of salt overload on left (LV) and right (RV) ventricular hypertrophy and fibrosis. Methods Male Wistar rats were fed normal‐ (NS ‐ NaCl = 1,27%, n=8) or high‐ (HS ‐ NaCl ...
Ellen Priscila Brito Dopona +3 more
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ChemInform Abstract: Organoboron Compounds. Part 21. Dialkylaminoethanethiophenylboranes.
Chemischer Informationsdienst, 1983AbstractDie Dialkylaminoethylthiophenylborane (III) werden durch Umsetzung von Chlorodialkylaminophenylboranen (I) mit Bleiethylthiolat (II) oder durch Reaktion von Bis‐(ethylthio)‐phenylboran (IV) mit einem sekundären Amin (V) dargestellt.
R. H. CRAGG, T. J. MILLER
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