硫代磷酰基

The thiophosphorylation reaction is a key step in the synthesis of organothiophosphorus compounds.
硫代磷酸化反应是有机硫磷化合物合成的关键步骤。
Thiophosphoryl chloride, also known as thionyl phosphorus chloride, is an important reagent in organic chemistry.
硫代磷酸氯是一种重要的有机化学试剂，也称为亚硫酰氯化磷。
Thiophosphoryl groups can replace phosphoryl groups in certain biochemical reactions, thus affecting signal transduction pathways.
在某些生化反应中，硫代磷酸基团可以替代磷酸基团，从而影响信号转导途径。
The thiophosphorylation of proteins has been studied as an alternative to phosphorylation for modifying enzyme activities.
蛋白质的硫代磷酸化作为一种替代磷酸化以修饰酶活性的方法已被研究。
In pesticide chemistry, thiophosphoryl derivatives are used as alternatives to phosphoryl compounds due to their reduced environmental impact.
在农药化学中，由于其对环境影响较小，硫代磷酸衍生物被用作磷酸化合物的替代品。
The introduction of a thiophosphoryl moiety can enhance the stability and selectivity of certain therapeutic agents.
引入硫代磷酸基团可以增强某些治疗药物的稳定性和选择性。
Thiophosphoryl azide is a high-energy compound that has applications in explosives and propellants.
硫代磷酸叠氮是一种具有高能量的化合物，在炸药和推进剂中有应用。
The sulfur atom in thiophosphoryl compounds makes them less susceptible to hydrolysis compared to their phosphoryl analogues.
与磷酸类似物相比，硫代磷酸化合物中的硫原子使其对水解的敏感性降低。
Studies have shown that some thiophosphorylated nucleotides can mimic the biological effects of naturally occurring phosphorylated nucleotides.
研究表明，一些硫代磷酸化的核苷酸能够模拟天然磷酸化核苷酸的生物学效应。
The synthesis of thiophosphoryl esters involves the reaction between an alcohol and thiophosphoryl chloride under basic conditions.
硫代磷酸酯的合成涉及醇与硫代磷酸氯在碱性条件下发生的反应。