2024-03-29T10:47:56Zhttps://repositori.uji.es/oai/requestoai:repositori.uji.es:10234/437092022-12-02T16:05:13Zcom_10234_7053com_10234_9col_10234_8639
00925njm 22002777a 4500
dc
Ribés Vidal, Celia
author
Falomir, Eva
author
Carda, Miguel
author
Marco, J. Alberto
author
2009
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.
Tetrahedron, 65, 34, p. 6965-6971
404020
http://hdl.handle.net/10234/43709
http://dx.doi.org/10.1016/j.tet.2009.06.046
Stereoselective syntheses of the glycosidase inhibitors hyacinthacine A2, hyacinthacine A3 and 5-epi-hyacinthacine A3