Relevant bibliographies by topics / Carbazoles (6H)

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Carbazoles (6H)'

Author: Grafiati
Published: 4 June 2021
Last updated: 16 February 2022

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Journal articles on the topic "Carbazoles (6H)"

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Singha, Raju, Atiur Ahmed, Yasin Nuree, Munmun Ghosh, and Jayanta K. Ray. "KOtBu mediated efficient approach for the synthesis of fused heterocycles via intramolecular O-/N-arylations." RSC Advances 5, no. 62 (2015): 50174–77. http://dx.doi.org/10.1039/c5ra07532g.

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Golubeva, I. S., N. P. Yavorskaya, L. V. Ektova, et al. "ANTITUMOR ACTIVITY OF SOME DERIVATIVES OF INDOLO[2,3-A]CARBAZOLES N-GLYCOSIDES WITH XYLOSE CARBOHYDRATE RESIDUE." Russian Journal of Biotherapy 19, no. 4 (2020): 86–93. http://dx.doi.org/10.17650/1726-9784-2020-19-4-86-93.

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Introduction. The search for new antineoplastic agents in a series of indolo[2,3-a]-carbazole derivatives is an urgent and promising direction, since compounds with antitumor activity have been found in this class. In the chemical fusion laboratory, N.N. Blokhin National Medical Research Center оf the Ministry of Health of Russia has developed an original and effective method for the synthesis of glycosides of indolo[2,3-a]-pyrrolo[3,4-c]carbazoles, which makes it possible to synthesize derivatives of N-glycosides of indolo[2,3-a]carbazoles with different substituents in the heterocyclic parts
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Modi, Sandeep P., Todd McComb, Abdel-Hadi Zayed, R. Christopher Oglesby, and Sydney Archer. "Synthesis of 6h-pyrido[4,3-b]carbazoles." Tetrahedron 46, no. 16 (1990): 5555–62. http://dx.doi.org/10.1016/s0040-4020(01)87753-x.

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MODI, S. P., T. MCCOMB, A. H. ZAYED, R. C. OGLESBY, and S. ARCHER. "ChemInform Abstract: Synthesis of 6H-Pyrido(4,3-b)carbazoles." ChemInform 22, no. 1 (2010): no. http://dx.doi.org/10.1002/chin.199101222.

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Yaqub, Ghazala, Abdul Hannan, Erum Akbar, et al. "Synthesis, Antibacterial, and Antifungal Activities of Novel Pyridazino Carbazoles." Journal of Chemistry 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/818739.

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Strategy to synthesize novel carbazole, that is, 2,3-dihydro-2-phenyl-6H-pyridazino[4, 5-b]carbazole-1,4-dione (2), is developed as key reaction. This novel compound showed ideal reactivity toward different functional groups like methyl, carboxylic, nitro, piperazine, and amine; thus series of its derivatives are synthesized sequentially with the aim to fuel up the carbazole compounds with new versatile derivatives. All compounds were investigated for their activity against bacteria (MRSA andS. typhi) and fungi (Candida albicans). Among tested compounds3,6, and8exhibited pronounced antibacteri
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Trécourt, François, Marc Mallet, Florence Mongin, and Guy Quéguiner. "Synthesis of 11H-Pyrido[2,3-a]carbazoles and 6H-Pyrido[3,2-b]carbazoles from 8-methoxy bromoquinolines." Tetrahedron 51, no. 43 (1995): 11743–50. http://dx.doi.org/10.1016/0040-4020(95)00726-o.

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Archer, Sydney, Bruce S. Ross, Livia Pica-Mattoccia, and Donato Cioli. "Synthesis and biological properties of some 6H-pyrido[4,3-b]carbazoles." Journal of Medicinal Chemistry 30, no. 7 (1987): 1204–10. http://dx.doi.org/10.1021/jm00390a014.

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Moinet-Hedin, V., T. Tabka, F. Sichel, et al. "In vitro cytotoxicity of carbazole derivatives. V. 9-Halogeno-substituted 5,11-dimethyl-6H-pyrido[3,2-b]carbazoles." European Journal of Medicinal Chemistry 32, no. 2 (1997): 113–22. http://dx.doi.org/10.1016/s0223-5234(97)87537-x.

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TRECOURT, F., M. MALLET, F. MONGIN, and G. QUEGUINER. "ChemInform Abstract: Synthesis of 11H-Pyrido(2,3-a)carbazoles and 6H-Pyrido(3,2-b) carbazoles from 8-Methoxy Bromoquinolines." ChemInform 27, no. 9 (2010): no. http://dx.doi.org/10.1002/chin.199609151.

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Modi, Sandeep P., Meged A. Michael, Sydney Archer, and James J. Carey. "An efficient synthesis of C-11 substituted 6H-pyrido[4,3-b]carbazoles." Tetrahedron 47, no. 33 (1991): 6539–48. http://dx.doi.org/10.1016/s0040-4020(01)82308-5.

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Dissertations / Theses on the topic "Carbazoles (6H)"

1

Jenkins, Paul D. "Studies towards the synthesis of functionalised 6H-pyrido[4,3-b]carbazoles." Thesis, University of Bath, 1989. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.328933.

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Chanel-Gillet, Brigitte. "Étude par résonance magnétique nucléaire à une et deux dimensions de quelques sucres, glycopeptides et oligonucléotides." Paris 11, 1985. http://www.theses.fr/1985PA112129.

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Le but de ce travail est d’étudier, par Résonance Magnétique Nucléaire à une et deux dimensions, la conformation en solution, de quelques glucides et de certains de leurs dérivés biologiques, en liaison avec leur réactivité chimique ou leurs caractéristiques biochimiques. La R. M. N. Dynamique permet d’évaluer sans modifier les molécules étudiées, la réactivité comparée des fonctions hydroxyle de monosaccharides. Les derniers développements de la R. M. N. 2D sont utilisés pour déterminer la structure tridimensionnelle, d’une part, de glycopeptides modèles de la Glycophorine A, et d’autre part,
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Letois, Bertrand. "Synthèse et étude physicochimique de nouveaux 5,11-diméthyl-6H-pyrido[3,2-b] carbazoles à visée antitumorale." Caen, 1991. http://www.theses.fr/1991CAEN4038.

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Moinet-Hedin, Véronique. "Contribution à l'étude du mécanisme d'action de nouvelles drogues à potentiel antitumoral dans la série des 5,11-diméthyl-6H-pyrido(3,2-b)carbazoles." Caen, 1994. http://www.theses.fr/1994CAEN4049.

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PRALY-DEPREZ, ISABELLE. "Synthese et etude de 11-amino-9-methoxy-5-methyl-6h-pyrido 4,3-b carbazoles et de 11-amino-5,6-dimethyl-5h-pyrido 3,4 : 4,5 pyrrolo 2,3-g isoquinoleines (nouveaux derives des ellipticines et 9-azaellipticines)." Paris 11, 1991. http://www.theses.fr/1991PA112094.

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Pour realiser la synthese des derives inedits de l'ellipticine nommes dans le titre, nous avons condense le 4-acetyl-n,n-diisopropylnicotinamide (obtenu en 4 etapes a partir de l'anhydride cynchomeronique) avec le 1-benzenesulfonyl-2-lithio-5-methoxyindole, ce qui nous a conduit au 4-1-(1-benzenesulfonyl-5-methoxyinol-2-yl)-1-hydroxyethyl-n,n-diisopropylnicotinamide. L'hydrolyse de l'amide et de la reduction de l'alcool fournissent ensuite l'acide 4-1-(1-benzenesulfonyl-5-methoxyindol-2-yl) ethyl nicotinique dont les amides sont cyclises pour conduire aux structures tetracycliques. Apres la de
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Journal articles
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