首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Selective synthesis of N,N,N-trimethylated chitosan derivatives at different degree of substitution and investigation of structure-activity relationship for activity against P. aeruginosa and MRSA
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Selective synthesis of N,N,N-trimethylated chitosan derivatives at different degree of substitution and investigation of structure-activity relationship for activity against P. aeruginosa and MRSA

机译:不同替代替代程度的N,N,N-三甲基化壳聚糖衍生物的选择性合成及对铜绿假单胞菌和MRSA的活性的研究 - 活性关系研究

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摘要

Two new cationic chitosan derivatives were synthesized using a combination of Boc and TBDMS protection strategies. This included a series of six samples of the TMC(NH2/TM )derivative, where some of the amino groups were N,N,N-trimethylated and the remaining was in the primary state. A series of six samples of the TACin derivative, where some of the amino groups were N-acetylated with quaternary 2-(N,N,N-trimethylammoniumyl) acetyl group and the remaining fully N-acetylated, were also synthesized. The degree of substitution (DS) for quaternary amino groups in these series ranged from 0.06-0.89. TMCDM/TM derivatives with a mix of N,N,N-trimethylated and N,N-dimethylated groups were also synthesized according to a published procedure but in this case, it was more difficult to control the DS than with the TBDMS protection strategy.
机译:使用BOC和TBDMS保护策略的组合合成了两种新的阳离子壳聚糖衍生物。 这包括一系列六个样品的TMC(NH 2 / TM)衍生物,其中一些氨基是N,N,N-三甲基化且其余在主要状态。 一系列六凝集蛋白衍生物的样品,其中一些氨基与季氨基化氨基化,也合成了季铵2-(N,N,N-三甲基铵基)乙酰基,并且还合成了剩余的完全正乙酰化。 这些系列中季氨基的替代度(DS)的取代度范围为0.06-0.89。 还根据公开的程序合成了具有N,N,N-三甲基化和N,N-二甲基化基团混合物的TMCDM / TM衍生物,但在这种情况下,更难以控制DS而不是TBDMS保护策略。

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