carbazole การใช้

• This enzyme participates in benzoate degradation via hydroxylation and carbazole degradation.
• In the third step, this compound is oxidized by red lead to carbazole itself.
• The metabolic pathways : benzoate degradation via hydroxylation, carbazole degradation, and nitrogen metabolism.
• Another classic is the Bucherer carbazole synthesis
• It is able to degrade carbazole, and as such, may be used in bioremediation.
• The Bucherer carbazole synthesis is a related organic reaction that uses sodium bisulfite as a reagent.
• The metabolic pathways : carbazole degradation, benzoate degradation via coa ligation, and acridone alkaloid biosynthesis.
• Fusion of two benzene rings gives rise to a third large family of compounds, respectively the acridine, dibenzothiophene, carbazole, and dibenzofuran.
• There are also purely structural classifications based on the presence of carbazole, ?-carboline or other units in the carbon skeleton of the alkaloid molecule.
• The metabolic pathways : benzoate degradation via hydroxylation, toluene and xylene degradation, 1, 4-dichlorobenzene degradation, carbazole degradation, and styrene degradation.
• In addition, both oxygen and nitrogen heterocyclic hydrocarbons, such as parent and alkyl homologues of carbazole, quinoline, and pyridine, are present in many crude oils.
• The metabolic pathways : phenylalanine metabolism, benzoate degradation via hydroxylation, biphenyl degradation, toluene and xylene degradation, 1, 4-dichlorobenzene degradation, fluorene degradation, carbazole degradation, and styrene degradation.
• The metabolic pathways : phenylalanine metabolism, benzoate degradation via hydroxylation, biphenyl degradation, toluene and xylene degradation, 1, 4-dichlorobenzene degradation, fluorene degradation, carbazole degradation, ethylbenzene degradation, and styrene degradation.
• "' Girinimbine "'is a carbazole alkaloid isolated from the curry tree ( " Murraya koenigii " ) along with the related alkaloids mahanimbine, koenimbine, isomahanine, mahanine, and others.
• For many years, the structure was assigned, incorrectly, as having a " linear structure " ( EC no . 228-767-9, CAS RN 6358-30-1 ) which differ in terms of the carbazole ring fusion.
• E . K . T . Sivakumar, Sathiyan G, Thangamuthu R and Sakthivel P,  Dicyanovinylene carbazole based A-D-A type small molecules for organic solar cell applications " Communicated in Synthetic Metals, 18.12.2015.
• E . K . T . Sivakumar, Govindasamy Sathiyan, Ramasamy Ganesamoorthy, RangasamyThangamuthu, Pachagoundar Sakthivel,  Synthesis and studies of carbazole based ( A-D-A ) polymers for organic solar cell applications Communicated in Polymer International, 13.02.2016
• ""'Nocardioides aromaticivorans " "'is a gram-positive non-motile bacterium from the genus " Nocardioides " thathas been isolated from a river contaminated with dioxin in Kanagawa, Japan . " Nocardioides aromaticivorans " has the ability to degrade dibenzofuran and carbazole.
• E . K . T . Sivakumar, GovindasamySathiyan, Kumar Ramakrishnana, Ramasamy Ganesamoorthy Rangasamy Thangamuthu, Pachagounder Sakthivel  Synthesis and characterization of fluorescence poly ( carbazole-thiazolo [ 5, 4-d ] thiazole ) copolymer and effect of different dopants Third International Workshop on Advanced Functional Nanomaterials ( 16-18 Dec 2015 ).
• E . K . T . Sivakumar, Sathiyan G, Ganesamoorthy R, Thangamuthu R and SakthivelP,  Synthesis and studies of carbazole based ( A-D-A ) polymers for organic solar cell applications Published in Souvenir,  Application of Nanostructured Materials for Energy and Environmental Technology, ISBN : 978-93-85436-91-8.