还原胺化

本文综述了模板DNA指导的多种类型的有机合成反应，包括还原胺化、亲核取代、Henry、Wittig烯化、光化学连接以及多步小分子的合成等反应；

The numerous types of DNA-templated organic synthesis , including reductive amination , nucleophilic substitution , Henry , Wittig olefination , photochemical ligation and multistep small-molecule synthesis , etc , are reviewed .

以苯丙酮酸（PPA）在Pd/C催化剂上还原胺化合成DL苯丙氨酸（Phe）。

Synthesis of DL phenylalanine ( Phe ) from phenylpyruvic acid ( PPA ) by reductive amination over Pd / C catalyst was studied .

聚丙烯表面的生物相容性修饰：表面氨基放大还原胺化接枝磷酰胆碱

Surface Amino Amplification and Graft with Phosphorylcholine by Reductive Amination

羰基化合物的还原胺化反应是有机合成中的重要反应。

Reductive amination of the carbonyl compounds is an important organic synthesis .

离子液体中芳香醛选择性还原胺化反应研究

Study on the Selective Reductive Amination of Aromatic Aldehydes in Ionic Liquids

苯丙酮酸在Pd/C催化剂上还原胺化合成DL-苯丙氨酸

Synthesis of DL-Phenylalanine from Phenylpyruvic Acid by Reduction Amination over Pd / C Catalyst

葡萄糖与甲胺还原胺化产物的高效液相色谱分析

The Analysis of Hydrogenation Products of Glucose and Methyl amine by High Performance Liquid Chromatographic

还原胺化反应的新进展

Recent Progress in Reductive Amination Reaction

用还原胺化法将磷酰胆碱醛共价接枝到表面氨基上获得了磷酰胆碱改性的聚丙烯薄膜。

Phosphorylcholine ( PC ) bearing al-dehyde functionality was covalently bonded with the surface amino group by reductive amination .

在还原胺化类催化加氢反应中，如何避免酮被还原成醇，也是工业化生产中面临的难题之一。

In reductive amination , how to avoid to turn ketones into alcohols is one of difficulties in industrialized manufacturing .

使用纯度较高的三丙酮胺有利于加氢和还原胺化反应的进行及产品的分离。

It was ascertained that triacetoneamine with higher purity would give good results on hydrogenation , amination and seperation of the product .

在合成芬氟拉明的工艺研究中，采用均匀设计方法安排试验，并通过微机运算求得定量方程，以此选择最后还原胺化反应的最佳工艺条件，使产率提高15%，获得了预期结果。

Using uniform design as an experimental design method , favorable result was obtained in the research of synthetic conditions of fenfluramine .

重点研究了还原胺化反应，发现该反应中一步法优于两步法，主要是因为一步法操作简单，处理过程少，损失小。

Reduction-animation reaction was especially studied and its two methods were compared in this article , finding that one-step reaction was better than two-steps ' for its easier operations and less loss .

方法以无水哌嗪为起始原料，经酰化、还原、胺化、成盐等反应制得盐酸特拉唑嗪。

METHODS Terazosin hydrochloride was synthesized from anhydro-piperazine via acylation , reduction , amination , salification etc.