58928-84-0Relevant academic research and scientific papers
Design and synthesis of 2,3,4,9-tetrahydro-1H-carbazole and 1,2,3,4-tetrahydro-cyclopenta[b]indole derivatives as non-nucleoside inhibitors of hepatitis C virus NS5B RNA-dependent RNA polymerase
Gopalsamy, Ariamala,Shi, Mengxiao,Ciszewski, Gregory,Park, Kaapjoo,Ellingboe, John W.,Orlowski, Mark,Feld, Boris,Howe, Anita Y. M.
, p. 2532 - 2534 (2006)
A novel class of HCV NS5B RNA dependent RNA polymerase inhibitors containing 2,3,4,9-tetrahydro-1H-carbazole and 1,2,3,4-tetrahydro-cyclopenta[b] indole scaffolds were designed and synthesized. Optimization of the aromatic region showed preference for 5,8
Carbazole acetic acid derivatives
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, (2008/06/13)
Tetrahydrocyclopent[b]indole-3-acetic acid, tetrahydrocarbazole-1-acetic acid and hexahydrocyclohept[b]-indole-6-acetic acid derivatives in which the carbon bearing alkyl, lower alkenyl or lower cycloalkyl are disclosed. The compounds are useful antiinflammatory agents and methods for their preparation and use are described.
Cycloalkanoindoles. I. Synthesis and antiinflammatory actions of some acidic tetrahydrocarbazoles, cyclopentindoles, and cycloheptindoles
Asselin,Humber,Dobson,et al.
, p. 787 - 792 (2007/10/05)
A novel series of acidic cycloalkanoindoles comprising tetrahydrocarbazole, cyclopentindole, and cycloheptindole 1 acetic acids has been synthesized via the Fischer indolization between a phenylhydrazine and a 1 alkyl 2 oxocycloalkaneacetic acid ester. Th
