Stereoselective syntheses of the glycosidase inhibitors hyacinthacine A2, hyacinthacine A3 and 5-epi-hyacinthacine A3
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Scholar |
Altres documents de l'autoria: Ribés Vidal, Celia; Falomir, Eva; Carda, Miguel; Marco, J. Alberto
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Mostra el registre complet de l'elementcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/7053
comunitat-uji-handle3:10234/8639
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http://dx.doi.org/10.1016/j.tet.2009.06.046 |
Metadades
Títol
Stereoselective syntheses of the glycosidase inhibitors hyacinthacine A2, hyacinthacine A3 and 5-epi-hyacinthacine A3Data de publicació
2009Editor
ElsevierISSN
404020Cita bibliogràfica
Tetrahedron, 65, 34, p. 6965-6971Tipus de document
info:eu-repo/semantics/articleResum
Stereoselective syntheses of the naturally occurring glycosidase inhibitors hyacinthacines A2 and A3 are reported. In the case of hyacinthacine A2, the pyrrolizidine system was created from an acyclic precursor via a ... [+]
Stereoselective syntheses of the naturally occurring glycosidase inhibitors hyacinthacines A2 and A3 are reported. In the case of hyacinthacine A2, the pyrrolizidine system was created from an acyclic precursor via a double cyclization procedure with a one-pot formation of two C-N bonds. In the case of hyacinthacine A3, the two C-N bonds were created in separate steps. In addition, the non-natural epimer at C-5 of hyacinthacine A3 was obtained. [-]
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info:eu-repo/semantics/restrictedAccess
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