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Targeting SIRT3 sensitizes glioblastoma to ferroptosis by promoting mitophagy and inhibiting SLC7A11. [PDF]
Li X+11 more
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Efficacy and Safety of Approximately 3 Years of Continuous Ozanimod in Moderately to Severely Active Ulcerative Colitis: Interim Analysis of the True North Open-label Extension. [PDF]
Danese S+18 more
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Synthesis of substituted indans as prostacyclin analogues
Journal of the Chemical Society, Perkin Transactions 1, 1984A route is described to the substituted indans (8) and (10), prepared as analogues of prostaglandin I2(prostacyclin). Two key steps in the synthesis involve the regiospecific attack of lithium salts from allylic sulphides onto indene oxides and, after ...
M. Phialas+3 more
semanticscholar +3 more sources
Vapor-pressure and enthalpy of vaporization of indan and five methyl-substituted indans
The Journal of Chemical Thermodynamics, 1978Abstract Vapor-pressure determinations were made for indan, 1,1-dimethylindan, 4,6-dimethylindan, 4,7-dimethylindan, 1,1,4,6-tetramethylindan, and 1,1,4,7-tetramethylindan. The results were used to obtain derived values of enthalpy of vaporization.
A. Osborn, D. W. Scott
semanticscholar +3 more sources
Macromolecular Symposia, 1995
AbstractCationic polymerisation of 1, 4‐diisopropenyl benzene, 1, 4‐(2‐chloro‐isopropyl)benzene and related compounds yields soluble polymers with repeating units of indan.High performance polymers with indan units are available via nucleophilic substitution of halogenated aromatic monomers containing a central indan element, which are synthesized from
Dazhong Yang+4 more
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AbstractCationic polymerisation of 1, 4‐diisopropenyl benzene, 1, 4‐(2‐chloro‐isopropyl)benzene and related compounds yields soluble polymers with repeating units of indan.High performance polymers with indan units are available via nucleophilic substitution of halogenated aromatic monomers containing a central indan element, which are synthesized from
Dazhong Yang+4 more
openaire +2 more sources
Journal of Medicinal Chemistry, 1994
The (E)-2-(4-pyridylmethylene)-1-indanones(E)-1-(E)-5[(E)-1,H;(E)-2,4- OCH3; (E)-3,5-OCH3; (E)-4,4-OH;(E)-5,5-OH] were obtained by aldol condensation of the corresponding 1-indanones with 4-pyridinecarboxaldehyde, and in case of the OH compound (E)-4 ...
R. Hartmann, H. Bayer, G. Grün
semanticscholar +1 more source
The (E)-2-(4-pyridylmethylene)-1-indanones(E)-1-(E)-5[(E)-1,H;(E)-2,4- OCH3; (E)-3,5-OCH3; (E)-4,4-OH;(E)-5,5-OH] were obtained by aldol condensation of the corresponding 1-indanones with 4-pyridinecarboxaldehyde, and in case of the OH compound (E)-4 ...
R. Hartmann, H. Bayer, G. Grün
semanticscholar +1 more source