Zobrazeno 1 - 7
of 7
pro vyhledávání: '"José Domingo Rivera-Ramírez"'
Autor:
Francisco Flores-Hernández, Tania Isabel Zárate-López, Marco Antonio Alcaráz-Cano, Jaime Escalante, José Domingo Rivera-Ramírez
Publikováno v:
Журнал органічної та фармацевтичної хімії, Vol 22, Iss 2, Pp 3-25 (2024)
Podophyllotoxin, its derivatives and structural analogues are an extensive group of aryl-tetralin-lignans of interest in pharmacology due to their promising anticancer and antitumor activity. The synthesis methods that have been proposed to date seek
Externí odkaz:
https://doaj.org/article/5df94ff1079f45a8a210458031e3c193
Autor:
Marina A. Ortega-Rojas, José Domingo Rivera-Ramírez, C. Gabriela Ávila-Ortiz, Eusebio Juaristi, Fernando González-Muñoz, Edmundo Castillo, Jaime Escalante
Publikováno v:
Molecules, Vol 22, Iss 12, p 2189 (2017)
The use of the solvent engineering has been applied for controlling the resolution of lipase-catalyzed synthesis of β-aminoacids via Michael addition reactions. The strategy consisted of the thermodynamic control of products at equilibrium using the
Externí odkaz:
https://doaj.org/article/7b43050cf08949a78afd97b561e489d6
Autor:
José Domingo Rivera-Ramírez
Publikováno v:
Open Journal of Philosophy. 10:374-387
Considering the two most applied ethical ideologies in science, the Value Neutrality and the Precautionary Principle, the latter is the ethical criterion that best fits the way in which chemistry has been developed and is currently executed. This wor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be4c7ca41f00c3cf69ffb77b09a69359
https://doi.org/10.4236/ojpp.2020.103025
https://doi.org/10.4236/ojpp.2020.103025
Publikováno v:
International Journal of Organic Chemistry. :10-22
A simple, efficient and low-cost methodology for the synthesis of α-aryl-α,β-unsaturated esters using paraformaldehyde as a source of carbon was developed. Factors that control reaction yields such as temperature, concentration and reaction time w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e15a8c61855abbc05dc9cadf820af396
https://doi.org/10.4236/ijoc.2019.91002
https://doi.org/10.4236/ijoc.2019.91002
Autor:
José Domingo Rivera-Ramírez, C. Gabriela Avila-Ortiz, Eusebio Juaristi, Marina A Ortega-Rojas, Edmundo Castillo, Jaime Escalante, Fernando González-Muñoz
Publikováno v:
Molecules, Vol 22, Iss 12, p 2189 (2017)
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules; Volume 22; Issue 12; Pages: 2189
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules; Volume 22; Issue 12; Pages: 2189
The use of the solvent engineering has been applied for controlling the resolution of lipase-catalyzed synthesis of β-aminoacids via Michael addition reactions. The strategy consisted of the thermodynamic control of products at equilibrium using the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::111e55f67a2901392e7db98533931f62
https://www.mdpi.com/1420-3049/22/12/2189
https://www.mdpi.com/1420-3049/22/12/2189
Autor:
Edmundo Castillo, Agustín López-Munguía, Jaime Escalante, Alain Marty, José Domingo Rivera-Ramírez
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic
Journal of Molecular Catalysis B: Enzymatic, 2015, 112, pp.76-82. ⟨10.1016/j.molcatb.2014.12.009⟩
Journal of Molecular Catalysis B: Enzymatic, Elsevier, 2015, 112, pp.76-82. ⟨10.1016/j.molcatb.2014.12.009⟩
Journal of Molecular Catalysis B: Enzymatic, 2015, 112, pp.76-82. ⟨10.1016/j.molcatb.2014.12.009⟩
Journal of Molecular Catalysis B: Enzymatic, Elsevier, 2015, 112, pp.76-82. ⟨10.1016/j.molcatb.2014.12.009⟩
Chemoselective synthesis of N-protected β-amino esters involving lipase-catalyzed aza-Michael additions and α,β-unsaturated precursors is mainly hampered by the two electrophilic sites present on these compounds. In order to control the chemoselec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::265d56c1e27cb2c435b9fa6c945b5672
https://hal.science/hal-01268997
https://hal.science/hal-01268997
