Stereospecific synthesis and mass spectrometry of 5,6-trans-epoxy-8Z,11Z,14Z-eicosatrienoic acid.

Stereospecific synthesis and mass spectrometry of 5,6-trans-epoxy-8Z,11Z,14Z-eicosatrienoic acid.
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5,6-反式环氧-8Z,11Z,14Z-二十碳三烯酸的立体定向合成和质谱分析。

DOI:
10.1016/j.bmcl.2005.04.030
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发表时间:
2005
期刊:
Bioorganic & medicinal chemistry letters.
影响因子:
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通讯作者:
Balazy,Michael
Balazy,Michael
中科院分区:
--
文献类型:
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作者:
Roy,Uzzal;Stark,RussellL;Joshua,Robert;Balazy,Michael

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以5,6-trans-arachidonic acid为原料,通过碘内酯化和碱性脱碘反应合成了5,6-trans-epoxyeicosatrienoic acid(5,6-trans-EET),沿着通过质谱(LC-MS,负离子)和核磁共振(NMR)进行了表征,并与5,6-cis-EET进行了比较。
A novel, facile synthesis of 5,6-trans-epoxyeicosatrienoic acid (5,6-trans-EET) from 5,6-trans-arachidonic acid by iodolactonization and alkaline de-iodation is described along with characterization by mass spectrometry (LC–MS, negative ions) and NMR and comparison with 5,6-cis-EET.