Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Alejandro Diéguez-Vázquez"'
Autor:
Isaac F. Yu, Jenna L. Manske, Alejandro Diéguez-Vázquez, Antonio Misale, Alexander E. Pashenko, Pavel K. Mykhailiuk, Sergey V. Ryabukhin, Dmitriy M. Volochnyuk, John F. Hartwig
Publikováno v:
Nature Chemistry. 15:685-693
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b59c6234dfc6ddcb10b9dd3bce9c94e5
https://doi.org/10.1038/s41557-023-01159-4
https://doi.org/10.1038/s41557-023-01159-4
Autor:
Maialen Alonso, Santiago Cañellas, Francisca Delgado, Marta Serrano, Alejandro Diéguez-Vázquez, José Enrique Gómez
Publikováno v:
Organic Letters. 25:771-776
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f393b9e4e3e88e2dc44f0d8332be2c9
https://doi.org/10.1021/acs.orglett.2c04226
https://doi.org/10.1021/acs.orglett.2c04226
Autor:
José Crecente-Campo, Alejandro Diéguez-Vázquez, C. Christoph Tzschucke, Sally McGrath, Steven V. Ley
Publikováno v:
ChemInform. 40
The AuCl3-catalyzed double hydroalkoxylation of conjugated 7-hydroxyheptynoates offers a convenient route for the synthesis of six-membered cyclic acetals, which are common substructures of polyketide natural products. When conjugated 6-hydroxyhexyno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::183b3ddc5fafb69fd29b31a866c39aeb
https://doi.org/10.1002/chin.200932135
https://doi.org/10.1002/chin.200932135
Publikováno v:
ChemInform. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74fd4b022cb23883266016dd63080f6f
https://doi.org/10.1002/chin.200816180
https://doi.org/10.1002/chin.200816180
Autor:
Matthew O'Brien, Alejandro Diéguez-Vázquez, Day-Shin Hsu, Steven V. Ley, Yukihito Sumino, Helmut Kraus
Publikováno v:
Organicbiomolecular chemistry. 6(7)
Azeotropic reflux chromatography (in which the eluent is continuously recycled by means of refluxing) was used to separate a mixture of spiroketal intermediates in the scale-up synthesis of spongistatin 1, leading to an improved separation and an app
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a4d78d43e8b06c5e0bc84f0288c591d
https://pubmed.ncbi.nlm.nih.gov/18362951
https://pubmed.ncbi.nlm.nih.gov/18362951
Autor:
Helmut Kraus, Alejandro Diéguez-Vázquez, Antoine Français, Richard A. J. Horan, James R. Frost, Takashi Tsunoda, Steven V. Ley, Matthew O'Brien, Alessandra Polara, Day-Shin Hsu, Nikla Baricordi
Publikováno v:
Chemical Science. 4:1989
An improved route to the EF fragment of the spongistatins has been developed and employed in a synthesis of spongistatin 2. The C48–C51 diene side chain, which lacks the chlorine substituent present in spongistatin 1, presented some compatibility i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2c8625435cf3cdf48ae1184433b63da
https://doi.org/10.1039/c3sc50304f
https://doi.org/10.1039/c3sc50304f