Stereoselective synthesis of a C1-C18 fragment of amphidinolides G and H
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Altres documents de l'autoria: García Fortanet, Jorge; Formentín, Pilar; Diaz-Oltra, Santiago; Murga, Juan; 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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INVESTIGACIONMetadades
Títol
Stereoselective synthesis of a C1-C18 fragment of amphidinolides G and HAutoria
Data de publicació
2013-04Editor
ElsevierCita bibliogràfica
GARCÍA‐FORTANET, Jorge, et al. Stereoselective synthesis of a C1−C18 fragment of amphidinolides G and H . Tetrahedron , 2013, 69.15: 3192-3196Tipus de document
info:eu-repo/semantics/articleVersió de l'editorial
http://www.sciencedirect.com/science/article/pii/S0040402013002883Paraules clau / Matèries
Resum
A stereoselective synthesis of a C1–C18 segment of the structure of the cytotoxic macrolides amphidinolides G and H is reported. The target compound was retrosynthetically disconnected into three fragments. In the ... [+]
A stereoselective synthesis of a C1–C18 segment of the structure of the cytotoxic macrolides amphidinolides G and H is reported. The target compound was retrosynthetically disconnected into three fragments. In the synthetic sense, connection of the fragments was made by means of a Stille coupling and a Julia–Kocienski olefination. Precursors from the chiral pool were used as the starting materials. [-]
Publicat a
Tetrahedron Volume 69, Issue 15, 15 April 2013Drets d'accés
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