本论文的另一部分工作是合成了L -脯氨酸衍生的系列手性磺酰胺配体。
In this thesis, the synthesis of series of chiral sulfonamide ligands which were derived from L-proline is our another part of work.
同时，还改进了对甲苯磺酰氯和对甲苯磺酰甘氨酸的合成方法。
The improved methods for the syntheses of tolylsulfonyl chloride and Np-tolysulfonyl amino acids have been described in this work.
合成了苯磺酰组氨酸，并进行了元素分析、红外等表征。
The N-benzenesulfonyl-histidine compound is synthesized and characterized by elemental analysis, infrared and X-ray diffraction study.
通过蛋白酶活性位点丝氨酸残基的磺酰化，不可逆的抑制丝氨酸蛋白酶。
Irreversibly inhibits serine proteases by sulfonylation of the serine residue in the active site of the protease.
通过蛋白酶活性位点丝氨酸残基的磺酰化，不可逆的抑制丝氨酸蛋白酶。
Irreversibly inhibits serine proteases by sulfonylation of the serine residue in the active site of the protease.
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