Synthesis and Characterization of Hybrid Dimeric Steroid Spiroketals
Martín A. Iglesias‐Arteaga, Martha C. Mayorquín‐Torres, Mauricio Maldonado‐Domínguez, Marcos Flores-Ãlamo
Abstract
Martín A. Iglesias‐Arteaga, Martha C. Mayorquín‐Torres, Mauricio Maldonado‐Domínguez, Marcos Flores-Ãlamo
Abstract
Abstract The synthesis of six dimeric spiroketals bearing an estradiol half fused to the 5α- or 5β-epimers of androstane, cholestane, and spirostane nuclei is described. The synthetic procedure comprises the Sonogashira coupling of different steroid alkynes with 2-iodoestradiol 17-monoacetate, followed by Pd-catalyzed spiroketalization. The structural characterization of the obtained hybrid dimers was performed using a combination of 1D and 2D NMR techniques, and was assisted by DFT calculations. Single crystal X-ray diffraction of one of the obtained compounds confirmed the proposed structures.
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Abstract The synthesis of six dimeric spiroketals bearing an estradiol half fused to the 5α- or 5β-epimers of androstane, cholestane, and spirostane nuclei is described. The synthetic procedure comprises the Sonogashira coupling of different steroid alkynes with 2-iodoestradiol 17-monoacetate, followed by Pd-catalyzed spiroketalization. The structural characterization of the obtained hybrid dimers was performed using a combination of 1D and 2D NMR techniques, and was assisted by DFT calculations. Single crystal X-ray diffraction of one of the obtained compounds confirmed the proposed structures.
Key concepts: Chemistry, Sonogashira coupling, Steroid, Androstane, Epimer, Cholestane, Characterization (materials science), Stereochemistry