Oxidation products of arachidonic acid I. The synthesis of methyl 8R, 11R, 15-trihydroxy-9S, 12-oxyeicosa-5Z, 13E-dienoate (19)

DOI: 10.1016/S0040-4039(00)78823-X

Source and publish data:

Tetrahedron Letters p. 1001 - 1004 (1980)

Update date:2022-08-02

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Authors:

Just, George

Luthe, Corinne

Oh, Hunseung

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Article abstract of DOI:10.1016/S0040-4039(00)78823-X

Diacetone glucose was converted in high yield to 3-deoxy-5-6-anhydro-1,2-0-isopropylidene-D-glucofuranose(3), which was transformed to title compound.³ Its mass spectrum confirms the structure of a naturally occurring oxidation product of arach

Full text of DOI:10.1016/S0040-4039(00)78823-X

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Product name:3-deoxy-1,2-O-isopropylidene-5,6-di-O-tosyl-α-D-ribo-hexofuranose

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