Goniodiol and 9-Deoxygoniopypyrone: Syntheses and Absolute Configurations

DOI: 10.1039/c39920001640

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1640 - 1641 (1992)

Update date:2022-07-31

Topics: Column chromatography Chiral center Stereochemistry Synthetic route Total synthesis Mass spectrometry (MS) Enantiomers Optical rotation High-performance liquid chromatography (HPLC) Nuclear Magnetic Resonance (NMR) X-ray crystallography Chiral Resolution Absolute Configuration Goniodiol 9-Deoxygoniopypyrone

Authors:

Tsubuki, Masayoshi

Kanai, Kazuo

Honda, Toshio

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Article abstract of DOI:10.1039/c39920001640

The absolute configurations of natural goniodiol and 9-deoxygoniopypyrone are confirmed as 1 and 2 respectively by enantioselective syntheses starting from (2S,3R)-1,2-O-isopropylidene-3-(2-furyl)glycerol 6.

Full text of DOI:10.1039/c39920001640

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