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首页> 外文期刊>Journal of the Chemical Society, Perkin Transactions 1 >Synthesis of myo-inositol 4,6-cyclic,1,5-trisphasphate, a conformationally restricted analogue of myo-inositol 1,4,5-trisphosphate
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Synthesis of myo-inositol 4,6-cyclic,1,5-trisphasphate, a conformationally restricted analogue of myo-inositol 1,4,5-trisphosphate

机译:肌肉肌醇4,6-环,1,5-三磷酸酯的合成,肌醇1,4,5-三磷酸构象受限的类似物

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摘要

Myo-Inositol 4,6-cyclic,1,5-trisphosphate 2 has been prepared starting from myo-inositol. The suitably protected intermediates, obtained by judicious selective protections and deprotections, have been phosphorylated. Final one-pot deprotection gives the expected, conformationally restricted, analogue of myo-inositol 1,4,5-trisphosphate. The physico-chemical behaviour of this derivative could explain its biological inactivity. [References: 18]
机译:从肌醇开始制备肌醇4,6-环,1,5-三磷酸2。通过明智的选择性保护和脱保护作用获得的适当保护的中间体已被磷酸化。最终的一锅脱保护得到了预期的,构象受限的肌醇1,4,5-三磷酸酯类似物。该衍生物的理化行为可以解释其生物惰性。 [参考:18]

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