Results 231 to 240 of about 16,908 (263)
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ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Zavgorodnii, V. +4 more
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AbstractFor Abstract see ChemInform Abstract in Full Text.
Zavgorodnii, V. +4 more
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Anti-Cancer Agents in Medicinal Chemistry, 2007
Natural and synthetic carbazoles, either in a pure substituted or in an annellated substituted form, represent an important and heterogeneous class of anticancer agents, which has grown considerably over the last two decades. Many carbazole derivatives have been tested for cyctotoxic activity, some of them have entered clinical trials, but only ...
Asche, Christian, Demeunynck, Martine
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Natural and synthetic carbazoles, either in a pure substituted or in an annellated substituted form, represent an important and heterogeneous class of anticancer agents, which has grown considerably over the last two decades. Many carbazole derivatives have been tested for cyctotoxic activity, some of them have entered clinical trials, but only ...
Asche, Christian, Demeunynck, Martine
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Current Medicinal Chemistry, 2009
Carbazole derivatives are well known for their various pharmacological activities, including anti-HIV, anticancer, antibacterial and antifungal activities. This review will focus on carbazoles that possess antifungal activity against Candida albicans, the major human fungal pathogen. In our search for new fungicidal compounds, we identified a series of
Karin, Thevissen +4 more
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Carbazole derivatives are well known for their various pharmacological activities, including anti-HIV, anticancer, antibacterial and antifungal activities. This review will focus on carbazoles that possess antifungal activity against Candida albicans, the major human fungal pathogen. In our search for new fungicidal compounds, we identified a series of
Karin, Thevissen +4 more
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ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
D P, Chakraborty, Shyamali, Roy
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AbstractFor Abstract see ChemInform Abstract in Full Text.
D P, Chakraborty, Shyamali, Roy
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Polypyromellitimides based on carbazole and substituted carbazoles
European Polymer Journal, 1982Abstract Polypyromellitimides have been synthesized from carbazole and N -benzylcarbazole by a two-step procedure involving ring-opening polyaddition with pyromellitic dianhydride and subsequent thermal cyclodehydration. The physicochemical, thermal and dielectric properties of the polymers have been studied. The various N -substituents, such as N
Mukul Biswas, Sukhendu K. Das
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Carbazole‐Dendronized Luminescent Radicals
Angewandte Chemie, 2023AbstractA series of carbazole‐dendronized tris(2,4,6‐trichlorophenyl)methyl (TTM) radicals have been synthesized. The photophysical properties of dendronized radicals up to the fourth generation were compared systematically to understand how structure–property relationships evolve with generation. The photoluminescence quantum yield (PLQY) was found to
Rui Xiaotian +11 more
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1991
The European dye stuff industry originally provided the main stimulus for development of the chemistry of carbazoles since the discovery of the first member of the group, carbazole (1) from coal tar in 1872 by Graebe and Glazer (35). The isolation of carbazole as a degradation product of strychnine (2) by Clemo and Perkin (18) in 1924 provided further ...
D P, Chakraborty, S, Roy
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The European dye stuff industry originally provided the main stimulus for development of the chemistry of carbazoles since the discovery of the first member of the group, carbazole (1) from coal tar in 1872 by Graebe and Glazer (35). The isolation of carbazole as a degradation product of strychnine (2) by Clemo and Perkin (18) in 1924 provided further ...
D P, Chakraborty, S, Roy
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Notiz über höhermolekulare Carbazol‐Derivate 1‐Oxy‐carbazol‐äther und 3‐ Alkylamino‐carbazole)
Chemische Berichte, 1951AbstractDie Darstellung von l‐Oxy‐carbazol‐äthern und 3‐Alkylamino‐carbazolen unter Verwendung von höheren linearen Alkylchloriden und ihre Eigenschaften werden beschrieben.
Hans Fürst, Joachim Bosse
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Carbazole substituted boron dipyrromethenes
Dalton Trans., 2014meso-N-Butylcarbazole substituted BODIPYs showed red shifted emission, large Stokes shifts and efficient energy transfer from the meso-carbazole unit to the BODIPY core.
Praseetha E, Kesavan, Iti, Gupta
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