Studies Toward the Total Synthesis of (+)-Providencin
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This book describes a convergent synthetic efforts toward the total synthesis of providencin, a marine natural product, which shows modest anticancer activity. This approach focus on efficient synthesis of two major fragments, which possess all the carbon atoms needed for providencin, followed by assembling them. The highlights of this approach are furanose-to-cyclobutane transformation, allenone-to-furan cycloisomerization, C-H activation, aldol reaction, and Stille-coupling.
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