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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