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Syntheses of 3H- and 2H-labeled (16S)-15-deoxy-16-hydroxy-16-methyl-5-thiaprostaglandin E1 methyl esters

✍ Scribed by Satoshi Sugiura; Toshio Tanaka; Kiyoshi Bannai; Seizi Kurozumi


Publisher
John Wiley and Sons
Year
1991
Tongue
French
Weight
498 KB
Volume
29
Category
Article
ISSN
0022-2135

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✦ Synopsis


Abstract

The syntheses of [7‐^2^H]‐, [7‐^3^H]‐, and [2,2,3,3,4,4‐^2^H~6~]‐(16__S__)‐15‐deoxy‐16‐ hydroxy‐16‐methyl‐5‐thiaprostaglandin E~1~ methyl ester (2, 3, and 4) are described. Both 7‐labeled compounds, 2 and 3, were prepared from the Δ^7^‐precursor (11) by treatment with in‐situ generated tributyltin deuteride and [^3^H]hydride, respectively. The hexa‐deuterated compound 4 was prepared starting from tetrahydrofuran‐d~8~


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