Synthesis of 4-Aryl-2-aminopyridine Derivatives and Related Compounds
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2009
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Metapodaci
Prikaz svih podataka o dokumentuApstrakt
A short, efficient, and high-yielding synthesis of 4-aryl-2-aminopyridine derivatives has been developed. The route employs two palladium-catalyzed processes, the Suzuki reaction and the Buchwald-Hartwig amination, as the key steps. The same approach has been used for preparation of the corresponding quinoline derivatives. In addition, a brief study of biological properties showed the anticancer potential of these compounds.
Ključne reči:
Aminopyridines / aminoquinolines / palladium catalysis / synthesisIzvor:
Tenside Surfactants Detergents, 2009, 39, 23, 4249-4263Izdavač:
- Taylor & Francis Inc, Philadelphia
Finansiranje / projekti:
- Sinteza, kvantitativni odnosi između strukture/osobina i aktivnosti, fizičko-hemijska karakterizacija i analiza farmakološki aktivnih supstanci (RS-MESTD-MPN2006-2010-142071)
DOI: 10.1080/00397910902898601
ISSN: 0039-7911
WoS: 000272207100010
Scopus: 2-s2.0-70350666376
Institucija/grupa
PharmacyTY - JOUR AU - Pavlović, Vladimir AU - Petković, Miloš AU - Popović, Stanimir AU - Savić, Vladimir PY - 2009 UR - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1209 AB - A short, efficient, and high-yielding synthesis of 4-aryl-2-aminopyridine derivatives has been developed. The route employs two palladium-catalyzed processes, the Suzuki reaction and the Buchwald-Hartwig amination, as the key steps. The same approach has been used for preparation of the corresponding quinoline derivatives. In addition, a brief study of biological properties showed the anticancer potential of these compounds. PB - Taylor & Francis Inc, Philadelphia T2 - Tenside Surfactants Detergents T1 - Synthesis of 4-Aryl-2-aminopyridine Derivatives and Related Compounds VL - 39 IS - 23 SP - 4249 EP - 4263 DO - 10.1080/00397910902898601 ER -
@article{ author = "Pavlović, Vladimir and Petković, Miloš and Popović, Stanimir and Savić, Vladimir", year = "2009", abstract = "A short, efficient, and high-yielding synthesis of 4-aryl-2-aminopyridine derivatives has been developed. The route employs two palladium-catalyzed processes, the Suzuki reaction and the Buchwald-Hartwig amination, as the key steps. The same approach has been used for preparation of the corresponding quinoline derivatives. In addition, a brief study of biological properties showed the anticancer potential of these compounds.", publisher = "Taylor & Francis Inc, Philadelphia", journal = "Tenside Surfactants Detergents", title = "Synthesis of 4-Aryl-2-aminopyridine Derivatives and Related Compounds", volume = "39", number = "23", pages = "4249-4263", doi = "10.1080/00397910902898601" }
Pavlović, V., Petković, M., Popović, S.,& Savić, V.. (2009). Synthesis of 4-Aryl-2-aminopyridine Derivatives and Related Compounds. in Tenside Surfactants Detergents Taylor & Francis Inc, Philadelphia., 39(23), 4249-4263. https://doi.org/10.1080/00397910902898601
Pavlović V, Petković M, Popović S, Savić V. Synthesis of 4-Aryl-2-aminopyridine Derivatives and Related Compounds. in Tenside Surfactants Detergents. 2009;39(23):4249-4263. doi:10.1080/00397910902898601 .
Pavlović, Vladimir, Petković, Miloš, Popović, Stanimir, Savić, Vladimir, "Synthesis of 4-Aryl-2-aminopyridine Derivatives and Related Compounds" in Tenside Surfactants Detergents, 39, no. 23 (2009):4249-4263, https://doi.org/10.1080/00397910902898601 . .