Zobrazeno 1 - 6
of 6
pro vyhledávání: '"R. Israel Hernández‐Benitez"'
Autor:
Edson Barrera, R. Israel Hernández‐Benitez, Carlos A. González‐González, Carlos H. Escalante, Aydeé Fuentes‐Benítes, Carlos González‐Romero, Elvia Becerra‐Martínez, Francisco Delgado, Joaquín Tamariz
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a9fb55861c1814d7c4a43e8efeed2e7
https://doi.org/10.1002/ejoc.202200364
https://doi.org/10.1002/ejoc.202200364
Autor:
R. Israel Hernández-Benitez, Edson Barrera, Vanessa Pelayo, Julio López, Miguel A. Vázquez, Joaquín Tamariz, Hugo A. Jiménez-Vázquez, Aydeé Fuentes-Benites, Blanca M. Santoyo, Carlos H. Escalante, Guadalupe Martínez‐Morales, Francisco Delgado, Daniel Zárate-Zárate, Carlos González-Romero
Publikováno v:
Chirality. 31:719-749
Enantiopure 3-((R)- and 3-((S)-1-phenylethyl)-4-oxazoline-2-ones were evaluated as chiral building blocks for the divergent construction of heterocycles with stereogenic quaternary centers. The N-(R)- or N-(S)-1-phenylethyl group of these compounds p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f223d98b7b77f7f392fcceeb3e027beb
https://doi.org/10.1002/chir.23109
https://doi.org/10.1002/chir.23109
Publikováno v:
Synthesis. 49:4357-4371
The scope and limitations of the strategy for the conversion of 2-anilinocyclohexenones and N-arylcyclohexane enaminones into the 1- and 2-oxygenated carbazole scaffolds, respectively, were evaluated. The one-pot palladium(0)-catalyzed aromatization/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ed1f6409c4da61288708ae3577d571e
https://doi.org/10.1055/s-0036-1588467
https://doi.org/10.1055/s-0036-1588467
Autor:
Daniel Zárate-Zárate, Francisco Delgado, Ehecatl M. Labarrios, Joaquín Tamariz, Raul Aguilar, R. Israel Hernández-Benitez
Publikováno v:
Tetrahedron. 71:6961-6978
Captodative alkene 1-acetylvinyl p-nitrobenzenecarboxylate 1a was evaluated for its reactivity in Lewis acid-catalyzed Michael additions with functionalized benzene rings and heterocycles, leading to diverse conjugated addition adducts. The hydrolysi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37df6c3427d16460978fb93cf7220727
https://doi.org/10.1016/j.tet.2015.07.010
https://doi.org/10.1016/j.tet.2015.07.010
Autor:
Raul Aguilar, Francisco Delgado, Joaquín Tamariz, Ehecatl M. Labarrios, Daniel Zárate-Zárate, R. Israel Hernández-Benitez
Publikováno v:
ChemInform. 47
The presented method is used in the synthesis of naturally occurring alkaloid actinopolymorphol B (XVa) which is further transformed into the alkaloid tanakine (XVII).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fc091b24e68df6593502e170f8b72ac
https://doi.org/10.1002/chin.201602122
https://doi.org/10.1002/chin.201602122
Autor:
R. Israel Hernández-Benitez, Héctor Quiroz-Florentino, Judit A. Aviña, Eleuterio Burgueño-Tapia, Joaquín Tamariz
Publikováno v:
Synthesis. 2011:1106-1112
The synthesis of the natural furan derivatives 5-{[(4-hydroxybenzyl)oxy]methyl}-2-furaldehyde and pichiafuran C is described. Diverse alternative synthetic approaches were developed for the preparation of these natural products. They were prepared th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51c76eb60e2ce747f851897c1f189690
https://doi.org/10.1055/s-0030-1258455
https://doi.org/10.1055/s-0030-1258455