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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Reactivity of 3H-1,2,4-dithiazole-3-thiones and 3H-1,2-dithiole-3-thiones as suiturizing agents for oligonucleotide synthesis
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Reactivity of 3H-1,2,4-dithiazole-3-thiones and 3H-1,2-dithiole-3-thiones as suiturizing agents for oligonucleotide synthesis

机译:3H-1,2,4-二噻唑-3-硫酮和3H-1,2-二硫代-3-硫酮作为适合寡核苷酸合成的试剂的反应性

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摘要

The reactivity of 5-amino-3H-1,2,4-dithiazole-3-thiones substituted at their amino group and 5-amino-3H-1,2-dithiole-3-thiones substituted at their amino group and C4 toward compounds containing P(III) atoms has been studied. N,N-Disubstituted-N'-(3-thioxo-3H-1,2,4-dithiazol-5-yl)methanimidamides were selected as novel efficient sulfur transfer reagents suitable for DNA and RNA synthesis.
机译:在氨基上取代的5-氨基-3H-1,2,4-二噻唑-3-硫酮与在氨基和C4取代的5-氨基-3H-1,2-二硫代-3-硫酮对化合物的反应性已经研究了含有P(III)原子的化合物。选择N,N-二取代-N′-(3-硫代-3H-1,2,4-二噻唑-5-基)甲亚酰胺作为适合DNA和RNA合成的新型高效硫转移试剂。

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