Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Carlos E. Puerto-Galvis"'
Publikováno v:
Actualidades Biológicas, Vol 34, Iss 96, Pp 126-127 (2012)
Externí odkaz:
https://doaj.org/article/8366f15e6a854d8baf1598afb35944be
Publikováno v:
Reactions, Vol 4, Iss 3, Pp 329-341 (2023)
We hereby describe an efficient method for the preparation of a series of new 1-substituted 1,2,3-triazole-based acetaminophen derivatives through a clean, good-yielding, simple, and expeditious procedure based on the O-propargylation reaction of the
Externí odkaz:
https://doaj.org/article/e2945f2d97104f81b48a5ffa66adb90b
Publikováno v:
Current Organic Synthesis. 20:546-559
Background: Quinoline and its derivatives have been shown to display a wide spectrum of biological properties, especially anticancer activity. Particularly, diverse potent anticancer drugs are based on the 4-phenoxyquinoline skeleton, acting as small
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9041ade3044e4e5ef4097b2215bd6d29
https://doi.org/10.2174/1570179419666220830090614
https://doi.org/10.2174/1570179419666220830090614
Autor:
Cristian Ochoa-Puentes, Carlos E. Puerto Galvis, Mario A. Macías, Vladimir V. Kouznetsov, Angelica Peñaranda
Publikováno v:
Synthesis. 54:1857-1869
A tandem approach was developed for the efficient synthesis of substituted chromeno[4,3-b]quinolines from arylamines and O-cinnamyl salicylaldehydes under metal-catalyst- and photosensitizer-free reaction conditions. Our protocol is based on an inexp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7acbd42a16da3518e7e851e39b437e3
https://doi.org/10.1055/a-1638-5030
https://doi.org/10.1055/a-1638-5030
Autor:
Arturo René Mendoza Salgado, Carlos Mario Meléndez, Carlos E. Puerto Galvis, Vladimir V. Kouznetsov
Publikováno v:
Current Organic Synthesis. 18:431-442
Background: Hexahydro-2H-pyrano[3,2-c]quinolines are known to have antibacterial, antifungal, and antitumor properties. Great efforts have been made to develop new synthetic methods that lead to the synthesis of valuable libraries. Extensive methodol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2414162196f6b7edcc9a319ffa599d05
https://doi.org/10.2174/1570179418666210113160949
https://doi.org/10.2174/1570179418666210113160949
Publikováno v:
New Journal of Chemistry. 45:1565-1572
The Bischler–Napieralski reaction of N-phenylethyl cinnamamides was investigated in acetonitrile and 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim]PF6). Strong effects on the nature of the isolated products were observed depending on the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0c2ebdf75413f7678b2a32baa5bed85
https://doi.org/10.1039/d0nj05235c
https://doi.org/10.1039/d0nj05235c
Publikováno v:
Synthesis. 53:547-556
Considering the current challenges of the A3 redox-neutral C1-alkynylation of tetrahydroisoquinolines (THIQs), we studied this synthetic tool under visible light photocatalysis and transition-metal catalysis in order to describe alternative reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa9626d6294e3d7b610e428cc3ab6f2a
https://doi.org/10.1055/s-0040-1707370
https://doi.org/10.1055/s-0040-1707370
Publikováno v:
The Journal of Organic Chemistry. 84:15294-15308
A five-step total synthesis of Dysoxylum alkaloids has been achieved using a biomimetic approach from zanthoxylamide protoalkaloids. The synthesis featured a direct amidation and a Bischler–Napiera...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62018257b9f0ac97d8d27fa10b1204ca
https://doi.org/10.1021/acs.joc.9b02093
https://doi.org/10.1021/acs.joc.9b02093
Autor:
Luz Karime Luna-Parada, Pedro Luis Sanabria Florez, Doris Natalia Rosado-Solano, Vladimir V. Kouznetsov, Mario Alberto Barón-Rodríguez, Carlos E. Puerto-Galvis, Andrés Felipe Zorro-González, Leonor Y. Vargas-Méndez
Publikováno v:
Journal of Agricultural and Food Chemistry. 67:9210-9219
The insecticidal and antifeedant activities of five 7-chloro-4-(1H-1,2,3-triazol-1-yl)quinoline derivatives were evaluated against the maize armyworm, Spodoptera frugiperda (J.E. Smith). These hybr...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3cd5ab81a00797366ed092f3a4a0d698
https://doi.org/10.1021/acs.jafc.9b01067
https://doi.org/10.1021/acs.jafc.9b01067
Publikováno v:
Synthesis. 51:1949-1960
A series of N-phenethylcinnamamides were subjected to the Bischler–Napieralski reaction to furnish diverse 1-styryl-3,4-dihydroisoquinolines. We noticed that the desired products were unstable when the reaction was performed under conventional solv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8148268b84d02f77c06295ff3a62138f
https://doi.org/10.1055/s-0037-1610684
https://doi.org/10.1055/s-0037-1610684