Zobrazeno 1 - 10
of 177
pro vyhledávání: '"José G. Santos"'
Autor:
Jackson J. Alcázar, Niklas Geue, Verónica Valladares, Alvaro Cañete, Edwin G. Pérez, Luis García-Río, José G. Santos, Margarita E. Aliaga
Publikováno v:
ACS Omega, Vol 6, Iss 15, Pp 10333-10342 (2021)
Externí odkaz:
https://doaj.org/article/781c8c3474d543ddaddadfffb6ae7b4d
Autor:
Jackson J. Alcázar, Edgar Márquez, Luis García-Río, Agustín Robles-Muñoz, Angélica Fierro, José G. Santos, Margarita E. Aliaga
Publikováno v:
Frontiers in Chemistry, Vol 10 (2022)
The incorporation of a guest, with different basic sites, into an organized system (host), such as macrocycles, could stabilize, detect, or promote the formation of a certain protomer. In this context, this work aimed to study the influence of cucurb
Externí odkaz:
https://doaj.org/article/31e661f0ad1a46d4a09a40b35cf4bfa7
Autor:
Gabriela Coutinho Idalgo, José G. Santos Lima Júnior, Lais Delli Nogueira, Heloisa Rosa, Camila Richieri Gomes, Juliana Cristina Marinheiro
Publikováno v:
Brazilian Journal of Infectious Diseases, Vol 25, Iss , Pp 101178- (2021)
Externí odkaz:
https://doaj.org/article/3f5fba533b814ab290a5d157c925b19e
Publikováno v:
ARKIVOC, Vol 2008, Iss 10, Pp 151-160 (2008)
Externí odkaz:
https://doaj.org/article/fb4192a9324747d8a2c6bd678560e620
Publikováno v:
Journal of Inclusion Phenomena and Macrocyclic Chemistry. 103:1-20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::227e566b6e4037fb292db820fd8e3e63
https://doi.org/10.1007/s10847-022-01172-z
https://doi.org/10.1007/s10847-022-01172-z
Autor:
Jackson J. Alcázar, Luis García-Río, Agustín I. Robles, Luis Dinamarca-Villarroel, Angélica Fierro, José G. Santos, Margarita E. Aliaga
Publikováno v:
Journal of Molecular Liquids. 381:121790
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f34047338cb65bf4f82be88723938dac
https://doi.org/10.1016/j.molliq.2023.121790
https://doi.org/10.1016/j.molliq.2023.121790
Autor:
Margarita E. Aliaga, José G. Santos, Luis García-Río, Jackson J. Alcázar, Alvaro Cañete, Edwin G. Pérez, Verónica Valladares, Niklas Geue
Publikováno v:
ACS Omega
ACS Omega, Vol 6, Iss 15, Pp 10333-10342 (2021)
ACS Omega, Vol 6, Iss 15, Pp 10333-10342 (2021)
A series of aromatic Schiff bases, featuring 7-diethylamino-coumarin and with five different substituents at an adjacent phenyl ring, were synthesized and characterized. With the aim of assessing the stability of these dyes in acidic medium, their hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfd4cf508f043febca83f7150e0d72eb
https://doi.org/10.1021/acsomega.1c00683
https://doi.org/10.1021/acsomega.1c00683
Publikováno v:
New Journal of Chemistry. 45:11495-11505
Nucleophilic substitution reactions of the title compounds have been investigated with a series of secondary alicyclic amines in several solvents. The solvent, amine, and electrophilic group effects on kinetics, mechanism and nucleofugality hierarchy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::563c5c2d58fc867b3f25775782e16cb9
https://doi.org/10.1039/d0nj05837h
https://doi.org/10.1039/d0nj05837h
Autor:
José G. Santos, Guillermo Quintero, Margarita E. Aliaga, Kevin Droguett, Paulina Pavez, Alvaro Cañete
Publikováno v:
Supramolecular Chemistry. 32:605-613
The inclusion of 7-diethylamino-coumarin derivatives, bearing an ethyl acetoacetate (CAM1) and a methyl β-ketodithioester moiety (CAM2) in the cavity of cucurbit[7]uril (CB7), leads to different interaction forms with mercuric ions (Hg2+). The inter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::425f8542aa21c97975c839a27be73361
https://doi.org/10.1080/10610278.2020.1856845
https://doi.org/10.1080/10610278.2020.1856845
Autor:
Jackson J. Alcázar, José G. Santos, Roberto Figueroa Guíñez, Paulina Pavez, Margarita E. Aliaga, Ricardo A. Tapia
Publikováno v:
Pure and Applied Chemistry. 92:97-106
A series of amino-acid based ionic liquids (Bmim[AA]s) have been synthesized and evaluated as catalysts, in aqueous solution. The results of a kinetic study of the thiol-Michael reaction of L-Cysteine with trans-β-nitrostyrene demonstrated the advan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a8e2357cc61b3be7383efc13184e775
https://doi.org/10.1515/pac-2019-0212
https://doi.org/10.1515/pac-2019-0212