SYNTHESIS OF NOVEL PROSTANOIDS HAVING A CYCLOPENTAFURAN STRUCTURE WITH A HEMITHIOACETAL SIDE CHAIN FROM AUCUBIN

DOI: 10.1246/cl.1980.175

Source and publish data:

Chemistry Letters p. 175 - 176 (1980)

Update date:2022-08-05

Topics: Deprotection Purification and characterization Verification of Biological Activity Protection of Hydroxyl Groups

Authors:

Ohno, Kiyotaka

Naruto, Masanobu

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Article abstract of DOI:10.1246/cl.1980.175

The titled prostanoids, methyl (Z)-7-<(3aR,5S,6R,6aR)-1-(2-substituted-2-hydroxyethylthio)-5-hydroxy-hexahydro-1H-cyclopentafuran-6-yl>-5-heptenoates, were prepared from aucubin via hemithioacetalization in construction of the alkyl-end (C13-C20) side

Full text of DOI:10.1246/cl.1980.175

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