Convergent, stereoselective syntheses of the glycosidase inhibitors broussonetines D and M
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Otros documentos de la autoría: Ribés Vidal, Celia; Falomir, Eva; Murga, Juan; Carda, Miguel; Marco, J. Alberto
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Título
Convergent, stereoselective syntheses of the glycosidase inhibitors broussonetines D and MFecha de publicación
2011-06-03Editor
Royal Society of ChemistryISSN
1477-0520Cita bibliográfica
RIBES, Celia, et al. Convergent, stereoselective syntheses of the glycosidase inhibitors broussonetines D and M. Organic & biomolecular chemistry, 2009, vol. 7, no 7, p. 1355-1360.Tipo de documento
info:eu-repo/semantics/articleVersión de la editorial
https://pubs.rsc.org/en/content/articlelanding/2009/ob/b821431j#!divAbstractPalabras clave / Materias
Resumen
The first syntheses of the polyhydroxylated alkaloids (iminosugars) broussonetines D and M
glycosidase inhibitors of the pyrrolidine class, have been performed in a convergent, stereocontrolled
way from D-serine as ... [+]
The first syntheses of the polyhydroxylated alkaloids (iminosugars) broussonetines D and M
glycosidase inhibitors of the pyrrolidine class, have been performed in a convergent, stereocontrolled
way from D-serine as the chiral starting material. A cross metathesis step was one key feature of the
synthesis. The versatility of the synthetic concept chosen permits the access to many members of this
compound family, both natural ones and analogues thereof [-]
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Organic & biomolecular chemistry, 2009, v. 7Derechos de acceso
© Royal Society of Chemistry 2009
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