Zobrazeno 1 - 10
of 30
pro vyhledávání: '"José Gustavo Ávila-Zárraga"'
Autor:
José Gustavo Ávila-Zárraga, Angel Josabad Alonso-Castro, Marco Martín González-Chávez, Perla Niño-Moreno, Roberto Martinez, Carmen Gámez-Gómez, Manuel García-Gamboa, Ana Cristina Miranda-Torres
Publikováno v:
Arkivoc. 2020:262-275
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d3ad314699eed5c563d432be59841b7
https://doi.org/10.24820/ark.5550190.p011.208
https://doi.org/10.24820/ark.5550190.p011.208
Autor:
Carlos Amador Bedolla, Mariano Sánchez Castellanos, Víctor Manuel Ugalde Saldívar, José Gustavo Ávila Zárraga, Ximena Varela Olvera, Laura Elizabeth Rivera Méndez
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b04f43d647ec022a7c9028953c6838c
https://doi.org/10.26226/morressier.616e5c2462ba8657678b134d
https://doi.org/10.26226/morressier.616e5c2462ba8657678b134d
Publikováno v:
Bioorganic Chemistry
Graphical abstract
Highlights • Synthesis. • New compounds. • Molecular docking. • In silico ADME/Tox profiling. • SARS CoV-2 main protease.
The virus SARS CoV-2, which causes the respiratory infection COVID-19, continues its spre
Highlights • Synthesis. • New compounds. • Molecular docking. • In silico ADME/Tox profiling. • SARS CoV-2 main protease.
The virus SARS CoV-2, which causes the respiratory infection COVID-19, continues its spre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::704efc3a3f16863ede70dfb0175c89ca
Autor:
Ana E. Torres, Carlos A. Velásquez, Cecilia Gómez-Pech, Fernando Colmenares, José Gustavo Ávila-Zárraga
Publikováno v:
Journal of Molecular Modeling. 27
Reactions for the palladium-catalyzed intramolecular cyclization of the o-bromoindole and the o-bromo-N-methyl-indole derivatives in the presence and absence of base (Cs2CO3) were explored through DFT calculations. For the base-free reactions, the pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2239faabb487315ec266ec70fa99d895
https://doi.org/10.1007/s00894-020-04638-4
https://doi.org/10.1007/s00894-020-04638-4
Autor:
Carlos A, Velásquez, Ana E, Torres, Cecilia, Gómez-Pech, José Gustavo, Ávila-Zárraga, Fernando, Colmenares
Publikováno v:
Journal of molecular modeling. 27(1)
Reactions for the palladium-catalyzed intramolecular cyclization of the o-bromoindole and the o-bromo-N-methyl-indole derivatives in the presence and absence of base (Cs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5708fb0d9de22625b416a8088ef1a066
https://pubmed.ncbi.nlm.nih.gov/33392849
https://pubmed.ncbi.nlm.nih.gov/33392849
Publikováno v:
Tetrahedron Letters. 58:981-984
A formal synthesis of the sesquiterpene parvifoline is described. The key step of the synthesis is an aromatic Cope rearrangement of a trans- 1-aryl-ethenylcyclobutancarbonitrile. It is in fact a ring-expansion type reaction with the advantage of ach
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c4e6dfb3870851ffedb6e443256fcfb
https://doi.org/10.1016/j.tetlet.2017.01.087
https://doi.org/10.1016/j.tetlet.2017.01.087
Publikováno v:
Synthetic Communications. 47:364-367
Several new 6-(alkylamine)-6H-dibenz[c,e][1,2]oxaphosphinine-6-oxides were prepared through a one-pot reaction, starting with 2-phenylphenol, phosphorus trichloride, and a Zn catalyst, to form 6-chloro-6H-dibenz[c,e][1,2]oxaphosphine. The alkylamine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6eb97e86448c86de9a76bb52d5a0562a
https://doi.org/10.1080/00397911.2016.1265651
https://doi.org/10.1080/00397911.2016.1265651
Publikováno v:
Tetrahedron Letters. 59:3077-3079
Puleganic amides display interesting insect-repellent properties. A new synthetic route to this type of amide was developed involving an organocatalytic cyclization and metal-catalyzed hydrogenation in a one-pot protocol. An eco-friendly oxidative am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20eb6fc7db182e41aef405e159272d77
https://doi.org/10.1016/j.tetlet.2018.06.067
https://doi.org/10.1016/j.tetlet.2018.06.067
Publikováno v:
Tetrahedron Letters. 56:5321-5323
(±)-ar-Tenuifolene was synthesized using a ring expansion mediated by a formal 1,3-alkyl shift reaction on a trans-1-aryl-2-propenyl-cyclobutancarbonitrile as the key step to generating the cyclohexene moiety. The conditions for this rearrangement a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e782946feaf8d97905b11ff697eb5425
https://doi.org/10.1016/j.tetlet.2015.07.087
https://doi.org/10.1016/j.tetlet.2015.07.087
Autor:
Adrián Vázquez Sánchez, José Gustavo Ávila-Zárraga, Mariano Sánchez Mendoza, Consuelo García Manrique
Publikováno v:
Educación Química. 24:347-350
(Reduction of nitro compounds using the Pd/H2N-NH2/Mw system)The reduction of nitro compounds to obtain the corresponding amines is one of the most useful reactions in organic synthesis. Of the various methods for achieving such reductions, those bas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf28cbbcf8eafb490e0b98ff9b041447
https://doi.org/10.1016/s0187-893x(13)72485-6
https://doi.org/10.1016/s0187-893x(13)72485-6