Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Angel Palillero-Cisneros"'
Autor:
Angel Palillero-Cisneros, Paola G. Gordillo-Guerra, Fernando García-Alvarez, Olivier Jackowski, Franck Ferreira, Fabrice Chemla, Joel L. Terán, Alejandro Perez-Luna
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 1443-1451 (2023)
We demonstrate that α-(aminomethyl)acrylates are suitable acceptors for 1,4-additions of dialkylzincs in aerobic conditions. The air-promoted radical–polar crossover process involves the 1,4-addition of an alkyl radical followed by homolytic subst
Externí odkaz:
https://doaj.org/article/e8be299227c5484aa98b9cb39ba0fbfe
Autor:
Angel Palillero-Cisneros, Blanca M. Cabrera-Vivas, Lidia Meléndez-Balbuena, Laura Morales-Lara
Publikováno v:
ECORFAN Journal-Ecuador. :1-6
The present project analyses the synthesis of three hydrazones with new structures by Green Chemistry, for its later spectroscopic characterization. Hydrazones are organic compounds with interesting properties, such as being solids with specific melt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef26b805717ea89a4a3b689bb1662b2a
https://doi.org/10.35429/eje.2019.11.6.1.6
https://doi.org/10.35429/eje.2019.11.6.1.6
Publikováno v:
Tetrahedron. 76:130838
A simple and practical method is reported for the synthesis of 3-(2-arylethylidene)isoindolin-1-ones and 3-(2-arylethylidene)isobenzofuran-1(3H)-ones, proceeding with good to excellent yields and (E:Z) selectivity. This methodology involves the seque
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7312dc2f9a4bbac715e303cdc6697aa8
https://doi.org/10.1016/j.tet.2019.130838
https://doi.org/10.1016/j.tet.2019.130838
Autor:
Joel L. Terán, Jorge R. Juárez, Paola Gordillo-Guerra, Dino Gnecco, Angel Mendoza, Angel Palillero-Cisneros, David M. Aparicio-Solano
Publikováno v:
Tetrahedron: Asymmetry. 26:95-101
A high yielding regio- and diastereoselective 7-endo 2,3-epoxyamides and 2,3-aziridine carboxamide cyclization is reported. Several aryl and alkyl trans-2,3-epoxyamides were reacted with BF3·OEt2 to afford the corresponding 4-hydroxy-5-alkyl/aryl-te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91b1685e28578380d51866d9dd11a5a5
https://doi.org/10.1016/j.tetasy.2014.12.004
https://doi.org/10.1016/j.tetasy.2014.12.004
Autor:
Dino Gnecco, Jorge R. Juárez, Paola Gordillo-Guerra, David M. Aparicio-Solano, Angel Palillero-Cisneros, Joel L. Terán, Angel Mendoza
Publikováno v:
ChemInform. 46
The title reaction gives the products in high yield and in a regio- and stereoselective manner.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::408043bf561dd20426b24da62ecd76c1
https://doi.org/10.1002/chin.201525215
https://doi.org/10.1002/chin.201525215