Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Angélica Salinas-Torres"'
Publikováno v:
Molbank, Vol 2022, Iss 2, p M1387 (2022)
The 1,2,3-Triazole derivatives containing the sulfonyl group have proved their biological importance in medicinal chemistry and drug design. In this sense, we describe the regioselective synthesis of 2-(phenylsulfonyl)-2H-1,2,3-triazole 3 in good yie
Externí odkaz:
https://doaj.org/article/7785bb61bad04d0ebd9cd499400d631b
Publikováno v:
Molbank, Vol 2021, Iss 2, p M1215 (2021)
The novel N-(3,5-bis(trifluoromethyl)benzyl)stearamide 3 was prepared in moderate yield by a solventless direct amidation reaction of stearic acid 1 with 3,5-bis(trifluoromethyl)benzylamine 2 at 140 °C for 24 h under metal- and catalyst-free conditi
Externí odkaz:
https://doaj.org/article/afcbd5b90e264130b2b02bf92b4c3ce7
Autor:
Diana Hurtado-Rodríguez, Angélica Salinas-Torres, Hugo Rojas, Diana Becerra, Juan-Carlos Castillo
Publikováno v:
RSC advances. 12(54)
2-Pyridone-containing heterocycles are considered privileged scaffolds in drug discovery due to their behavior as hydrogen bond donors and/or acceptors and nonpeptidic mimics, and remarkable physicochemical properties such as metabolic stability, sol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02afcf839e5bb0b8b6c414b38138246c
https://pubmed.ncbi.nlm.nih.gov/36540221
https://pubmed.ncbi.nlm.nih.gov/36540221
Autor:
Angélica Salinas-Torres, Elizabeth Jiménez, Diana Becerra, José J. Martínez, Hugo Rojas, Juan-Carlos Castillo, Mario A. Macías
Publikováno v:
Journal of Molecular Structure. 1274:134414
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fabf846c6881d7d3f692b4882d8a1fd0
https://doi.org/10.1016/j.molstruc.2022.134414
https://doi.org/10.1016/j.molstruc.2022.134414
Publikováno v:
Molbank, Vol 2021, Iss M1215, p M1215 (2021)
The novel N-(3,5-bis(trifluoromethyl)benzyl)stearamide 3 was prepared in moderate yield by a solventless direct amidation reaction of stearic acid 1 with 3,5-bis(trifluoromethyl)benzylamine 2 at 140 °C for 24 h under metal- and catalyst-free conditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08b98c045931e44c59117ce84574b075
https://www.mdpi.com/1422-8599/2021/2/M1215
https://www.mdpi.com/1422-8599/2021/2/M1215