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Título

One-pot synthesis and SAR study of cis-2,6-dialkyl-4-chloro-tetrahydropyrans

AutorMiranda, Pedro O. CSIC ORCID ; León, Leticia G.; Martín, Víctor S. CSIC ORCID; Padrón, Juan I. CSIC ORCID ; Padrón, José M.
Palabras claveMarine drugs
Halogenated tetrahydropyrans
Solid tumors
Drug design
Structure–activity relationship
Fecha de publicación15-jun-2006
EditorElsevier
CitaciónBioorganic and Medicinal Chemistry Letters 16(12): 3135-3138 (2006)
ResumenA series of cis-2,6-dialkyl-4-chloro-tetrahydropyrans were prepared by means of an iron(III)-catalyzed process. The in vitro antiproliferative activities were examined in the human solid tumor cell lines A2780, SW1573, and WiDr. The results show that the presence of bulky substituents favors the Prins cyclization leading to new products with better activity profile against all cell lines tested.
Versión del editorhttps://doi.org/10.1016/j.bmcl.2006.03.064
URIhttp://hdl.handle.net/10261/212262
DOI10.1016/j.bmcl.2006.03.064
ISSN0960-894X
E-ISSN1464-3405
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