A stereocontrolled synthesis of (±)-1,6,7-trideoxyforskolin
Abstract
An efficient entry to c-ring annulation and subsequent elaboration in the synthesis of forskolin is described.
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Article information
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- Paper
J. Chem. Soc., Chem. Commun., 1987, 24-25
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A stereocontrolled synthesis of (±)-1,6,7-trideoxyforskolin
S. Hashimoto, M. Sonegawa, S. Sakata and S. Ikegami, J. Chem. Soc., Chem. Commun., 1987, 24 DOI: 10.1039/C39870000024
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