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首页> 外文期刊>Journal of the American Chemical Society >Model Reactions of Thyroxine Biosynthesis. Identification of the Key Intermediates in Thyroxine Formation from 3,5-Diiodo-L-tyrosine and 4-Hydroxy-3,5-diiodophenylpyruvic Acid
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Model Reactions of Thyroxine Biosynthesis. Identification of the Key Intermediates in Thyroxine Formation from 3,5-Diiodo-L-tyrosine and 4-Hydroxy-3,5-diiodophenylpyruvic Acid

机译:甲状腺素生物合成的模型反应。 3,5-二碘-L-酪氨酸和4-羟基-3,5-二碘苯基丙酮酸在甲状腺素形成中的关键中间体的鉴定

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摘要

In conclusion, we have isolated and rigorously characterized the reactive intermediates involved in thyroxine formation during the oxygenation of DIHPPA. Our study constitutes the first conclusive experimental proof that the intermediate is not 3-(4- hydroxy-3, 5-diiodophenyl)-3-hydroperoxy-2-oxopropionic acid (1) as was claimed, but rather it is the epoxides 8a and 9.
机译:总之,我们已经分离并严格表征了DIHPPA氧化过程中参与甲状腺素形成的反应性中间体。我们的研究构成了第一个结论性实验证据,表明该中间体不是3-(4-羟基-3,5-二碘苯基)-3-氢过氧-2-氧代丙酸(1),而是环氧化物8a和9。

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