Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jana Sendra"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 477-486 (2023)
The contribution to the energy barrier of a series of tethers in transannular cycloadditions of cycloalkenes with hydrazones has been computationally studied by using DFT. The Houk's distortion model has been employed to evaluate the influence of the
Externí odkaz:
https://doaj.org/article/3fcec1dd78d24d579e737e7584775486
Autor:
Jana Sendra, Oriol Salvado, Manuel Pedrón, Efraim Reyes, Tomás Tejero, Elena Fernández, Pedro Merino, Jose L. Vicario
The ability of cyclooctatetraene oxide to undergo two sequential ring contraction events under mild conditions, using Brønsted acid catalysis, has been studied in detail. We have found that the selectivity can be controlled by the acidity of the cat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24dead3872b1001ed1900478ecac8b86
http://zaguan.unizar.es/record/125977
http://zaguan.unizar.es/record/125977
Autor:
Elena Fernández Gutiérrez, Jose Luis Vicario Hernando, Liher Prieto Aretxabaleta, Efraim Reyes Martín, Jana Sendra
Publikováno v:
Organic Letters
Addi. Archivo Digital para la Docencia y la Investigación
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Addi. Archivo Digital para la Docencia y la Investigación
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[EN]Hydrazones derived from cycloalkenones undergo an enantioselective transannular formal (3 + 2) cycloaddition catalyzed by a chiral phosphoric acid. The reaction provides high yields and excellent stereocontrol in the formation of complex adducts
Publikováno v:
Angewandte Chemie (International ed. in English). 59(5)
Medium-sized carbocycles containing an α,β-unsaturated ketone moiety as Michael acceptor site and a ketone moiety as internal electrophilic site are ideal substrates to conduct Cu(I)-catalyzed conjugated borylation followed by electrophilic intramo
Autor:
Elena Fernández, Jorge J. Carbó, Jose L. Vicario, Efraim Reyes, Lorena García, Núria Miralles, Jana Sendra
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 24(53)
Complete stereocontrol on the transition-metal-free hydroboration of the distal double bond of allenamides could be achieved when allenamides contained acetyl substituents, which provided exclusively the Z-isomer. The consecutive Pd-catalyzed cross-c