Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Eugenia Aldeco-Pérez"'
Autor:
Lilian I. Olvera, Eugenia Aldeco-Pérez, Arturo Rico-Zavala, Luis G. Arriaga, José A. Ávila-Niño, Jorge Cárdenas, Rubén Gaviño, Karina S. Pérez, Victor H. Lara
Publikováno v:
Polymer Testing, Vol 95, Iss , Pp 107092- (2021)
Novel anion exchange membranes (AEMs) were synthesized by superacid-catalyzed step-growth polycondensation of isatine and p-terphenyl at room temperature. The materials obtained were functionalized by a highly efficient nucleophilic substitution reac
Externí odkaz:
https://doaj.org/article/6e1e2af2fd19429e8feb2bd4d53c8e5f
Publikováno v:
The Scientific World Journal, Vol 2013 (2013)
A library of 1,2,3-triazoles was synthesized from diverse alkynes and azides using catalytic amounts of silver chloride instead of copper compounds. In addition, a novel “abnormal” silver N-heterocyclic carbene complex was tested as catalyst in t
Externí odkaz:
https://doaj.org/article/597ec6b25c77482a8f83f967fcdca92c
Autor:
J.A. Ávila-Niño, Victor H. Lara, Arturo Rico-Zavala, Karina S. Pérez, Jorge Cárdenas, Eugenia Aldeco-Pérez, Lilian I. Olvera, Rubén Gaviño, Luis Gerardo Arriaga
Publikováno v:
Polymer Testing, Vol 95, Iss, Pp 107092-(2021)
Novel anion exchange membranes (AEMs) were synthesized by superacid-catalyzed step-growth polycondensation of isatine and p-terphenyl at room temperature. The materials obtained were functionalized by a highly efficient nucleophilic substitution reac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49ecb35cb0102280903aaae5588e72a1
https://doi.org/10.1016/j.polymertesting.2021.107092
https://doi.org/10.1016/j.polymertesting.2021.107092
Autor:
Cecilio Alvarez, Patrick Herson, María Teresa Ramírez Apan, Alfredo Toscano, Eugenia Aldeco-Pérez, Henri Rudler, A. Parlier
Publikováno v:
Tetrahedron Letters. 47:9053-9056
A series of dihydrobenzofuran-2-one 3 have been submitted to various dienophiles: whereas maleic anhydride led only to the adducts 4a , b , singlet oxygen gave the expected new endoperoxide lactones 5a – d , 6 and 7a , b , three of them showing int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5660a83a41183f7e62939b2d04138cc
https://doi.org/10.1016/j.tetlet.2006.10.093
https://doi.org/10.1016/j.tetlet.2006.10.093
Publikováno v:
Tetrahedron Letters. 47:4553-4556
2-Phenylpyridine activated by chromium tricarbonyl reacts with bis(TMS) ketene acetals to give pyridine-substituted bicyclic γ-lactones. On the other hand, its reaction with the same acetals leads, upon activation with methylchloroformate, to dihydr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::090aec7f6fd5edf9c84af8d41789756e
https://doi.org/10.1016/j.tetlet.2006.05.006
https://doi.org/10.1016/j.tetlet.2006.05.006
Autor:
Henri Rudler, Eugenia Aldeco-Pérez, Andrée Parlier, Cecilio Álvarez, Patrick Chaquin, Patrick Herson, Alfredo Toscano, María-Teresa Ramírez-Apan
Publikováno v:
Universidad Nacional Autónoma de México
UNAM
Redalyc-UNAM
Journal of the Mexican Chemical Society (México) Num.2 Vol.52
UNAM
Redalyc-UNAM
Journal of the Mexican Chemical Society (México) Num.2 Vol.52
"Arenechromium and cycloheptatrienechromium complexes react with (TMS)ketene acetals to give upon a double nucleophilic addition either diene-lactones or cyclohexenone-lactones. In the first case, the scope of the reaction and the stability of the di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::23928a20523b11d3b9bf774994080c84
https://www.redalyc.org/articulo.oa?id=47516171009
https://www.redalyc.org/articulo.oa?id=47516171009
Publikováno v:
Tetrahedron Letters. 47:8629
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0722a679612758f9915b29d5d16c21e7
https://doi.org/10.1016/j.tetlet.2006.09.074
https://doi.org/10.1016/j.tetlet.2006.09.074