80783-13-7Relevant academic research and scientific papers
A tris-pyrazolylborate ligand with hemilabile O-donor groups. Examples of η3, η5, η6 and bridging modes of bonding to Li+, Na+, K+, Tl+ and Ca2+ ions
Chisholm, Malcolm H.,Gallucci, Judith C.,Yaman, Guelsah
, p. 1872 - 1874 (2006)
A tris-pyrazolylborate ligand bearing ether appendages is shown to be a potential hemilabile ligand based on NMR studies and structural characterization of its η3, η5, η6, and μ-binding modes in coordination with Li+, Na+, K +, Tl+, and Ca2+ ions. The Royal Society of Chemistry 2006.
COMBINATION THERAPY OF AN HBSAG INHIBITOR AND AN INTERFERON
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, (2017/07/27)
The present invention is directed to compositions and methods for treating hepatitis B virus infection. In particular, the present invention is directed to a combination therapy comprising administration of an HBsAg inhibitor and an interferon for use in the treatment or prophylaxis of chronic Hepatitis B virus infections.
COMBINATION THERAPY OF AN HBSAG INHIBITOR AND AN HBV CAPSID ASSEMBLY INHIBITOR
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, (2017/07/14)
The present invention is directed to compositions and methods for treating hepatitis B virus infection. In particular, the present invention is directed to a combination therapy comprising administration of an HBs Ag inhibitor and an HBV capsid assembly inhibitor for use in the treatment or prophylaxis of chronic hepatitis B infected patients.
NOVEL 6,7-DIHYDROBENZO[A]QUINOLIZIN-2-ONE DERIVATIVES FOR THE TREATMENT AND PROPHYLAXIS OF HEPATITIS B VIRUS INFECTION
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Page/Page column 34; 35, (2016/06/01)
The invention provides novel compounds having the general formula (I) wherein R1 to R6, W and X are as described herein and their pharmaceutically acceptable salt, enantiomer or diastereomer thereof, and compositions including the compounds and methods of using the compounds.
4-Substituted 3,3-dimethyl-butan-2-ones, processes for their preparation and their use as intermediate products
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, (2008/06/13)
4-substituted 3,3-dimethyl-butan-2-ones of the formula STR1 in which R represents cyano or the grouping --X--R1, wherein R1 represents n-alkyl with 1 to 4 carbon atoms, isopropyl, isobutyl, sec.-butyl, alkenyl with 3 to 4 carbon atom
