Publikation: Facile Synthesis of Fluorinated Benzofuro- and Benzothieno[2,3-b]pyridines, α-Carbolines and Nucleosides Containing the α-Carboline Framework
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2009
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Synthesis. Georg Thieme Verlag. 2009, 2009(14), pp. 2393-2402. ISSN 0039-7881. eISSN 1437-210X. Available under: doi: 10.1055/s-0029-1217396
Zusammenfassung
Fluorinated benzofuro[2,3-b]pyridines, benzothieno[2,3-b]pyridines and 9H-pyrido[2,3-b]indoles (α-carbolines) were synthesized via regiospecific pyridine core annulation of a number of fluoro-containing 1,3-CCC-dielectrophiles to benzofuran-2-amine, benzothiophen-2-amine and 1H-indol-2-amine. Based on the 2,4-bis(trifluoromethyl)-9H-pyrido[2,3-b]indole thus synthesized, the preparative approach towards a set of nucleosides and nucleoside mimetics bearing the α-carboline framework was elaborated.
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IAROSHENKO, Viktor O., Yan WANG, Biao ZHANG, Dmitriy VOLOCHNYUK, Vyacheslav SOSNOVSKIKH, 2009. Facile Synthesis of Fluorinated Benzofuro- and Benzothieno[2,3-b]pyridines, α-Carbolines and Nucleosides Containing the α-Carboline Framework. In: Synthesis. Georg Thieme Verlag. 2009, 2009(14), pp. 2393-2402. ISSN 0039-7881. eISSN 1437-210X. Available under: doi: 10.1055/s-0029-1217396BibTex
@article{Iaroshenko2009Facil-58009,
year={2009},
doi={10.1055/s-0029-1217396},
title={Facile Synthesis of Fluorinated Benzofuro- and Benzothieno[2,3-b]pyridines, α-Carbolines and Nucleosides Containing the α-Carboline Framework},
number={14},
volume={2009},
issn={0039-7881},
journal={Synthesis},
pages={2393--2402},
author={Iaroshenko, Viktor O. and Wang, Yan and Zhang, Biao and Volochnyuk, Dmitriy and Sosnovskikh, Vyacheslav}
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<dcterms:abstract xml:lang="eng">Fluorinated benzofuro[2,3-b]pyridines, benzothieno[2,3-b]pyridines and 9H-pyrido[2,3-b]indoles (α-carbolines) were synthesized via regiospecific pyridine core annulation of a number of fluoro-containing 1,3-CCC-dielectrophiles to benzofuran-2-amine, benzothiophen-2-amine and 1H-indol-2-amine. Based on the 2,4-bis(trifluoromethyl)-9H-pyrido[2,3-b]indole thus synthesized, the preparative approach towards a set of nucleosides and nucleoside mimetics bearing the α-carboline framework was elaborated.</dcterms:abstract>
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