Regioselective phosphorylation of vicinal 3,4-hydroxy myo-inositol derivative promoted practical synthesis of d-PtdIns(4,5)P2 and d-Ins(1,4,5)P3
β Scribed by Fushe Han; Minoru Hayashi; Yutaka Watanabe
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 304 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
The reactivity of 3 and 4-OH in 3,4-diol myo-inositol derivatives were observed through the phosphorylation, acylation and silylation. The results indicated that 3-OH is much more reactive than 4-OH, giving regiospecifically 3-mono-functionalized products. This investigation provided a concise methodology for the synthesis of natural D-form of PtdIns(4,5)P2 and D-Ins(1,4,5)P3 from L-1,2-Ocyclohexylidene-3,4-O-(tetraisopropyl disiloxane-1,3-diyl)-myo-inositol.
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