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

方法以无水哌嗪为起始原料,经、还原、胺、成等反应制得酸特拉唑嗪。

The chemical modification methods of food proteins are summarized,including acylation,deamidation,phosphorylation,glycosylation,covalent cross-linking effect etc.

综述了、去胺、磷酸、糖基、共价交联等食品蛋白质的学改性技术及方法。

Method The target compound was synthesized from clarithromycin via hydrolyzation,acetylation,cyclic carbonatation,oxidation,decarbonatation,acylation,cyclic carbamatation and cyclization.

方法以克拉霉素为起始原料,经水解、乙、碳酸酯、氧、脱碳酸酯、、氨基甲酸酯和合等反应合成目标合物。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏基反应引入乙基，接着溴、胺，得到标题树脂。该法避免了使氯甲醚。

Acylation activity of hydroxyl groups in methyl cholicate has been determined by the use of methacryloyl chloride, methacryloyl anhydride and methacrylic acid as the acylating agents.

以甲基丙烯氯、甲基丙烯酸酐和甲基丙烯酸剂，研究了胆酸甲酯分子中羟基的反应活性。

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

方法以无为起始原料,经、还原、胺、成等反应制得酸特拉唑。

The chemical modification methods of food proteins are summarized,including acylation,deamidation,phosphorylation,glycosylation,covalent cross-linking effect etc.

综述作用、去胺作用、磷酸作用、糖基作用、共价交联作用等食品蛋白质的学改性技术及方法。

Method The target compound was synthesized from clarithromycin via hydrolyzation,acetylation,cyclic carbonatation,oxidation,decarbonatation,acylation,cyclic carbamatation and cyclization.

方法以克拉霉素为起始原料,经解、乙、环碳酸酯、氧、脱碳酸酯、、环氨基甲酸酯和环合等反应合成目标合物。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏基反应引入乙基，接着溴、胺，得到标题树脂。该法避免使用氯甲醚。

Acylation activity of hydroxyl groups in methyl cholicate has been determined by the use of methacryloyl chloride, methacryloyl anhydride and methacrylic acid as the acylating agents.

以甲基丙烯氯、甲基丙烯酸酐和甲基丙烯酸作剂，研究胆酸甲酯分子中羟基的反应活性。

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

方法以无水哌嗪为起始原料,经酰化、还原、胺化、成等反应制得酸特拉唑嗪。

The chemical modification methods of food proteins are summarized,including acylation,deamidation,phosphorylation,glycosylation,covalent cross-linking effect etc.

综述了酰化、去酰胺、磷酸化、基化、共价交联等食品蛋白质化学改性技术及方法。

Method The target compound was synthesized from clarithromycin via hydrolyzation,acetylation,cyclic carbonatation,oxidation,decarbonatation,acylation,cyclic carbamatation and cyclization.

方法以克拉霉素为起始原料,经水解、乙酰化、环碳酸酯化、氧化、脱碳酸酯化、酰化、环氨基甲酸酯化和环等反应成目标化物。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏酰基化反应引入乙酰基，接着溴化、胺化，得到标题树脂。该法避免了使氯甲醚。

Acylation activity of hydroxyl groups in methyl cholicate has been determined by the use of methacryloyl chloride, methacryloyl anhydride and methacrylic acid as the acylating agents.

以甲基丙烯酰氯、甲基丙烯酸酐和甲基丙烯酸酰化剂，研究了胆酸甲酯分子中羟基反应活性。

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

方法以无水哌嗪为起始原料,经酰化、还原、胺化、成等反应制得酸特拉唑嗪。

The chemical modification methods of food proteins are summarized,including acylation,deamidation,phosphorylation,glycosylation,covalent cross-linking effect etc.

综述了酰化、去酰胺、酸化、糖基化、共价交联等食品蛋白质的化学改性技术及方法。

Method The target compound was synthesized from clarithromycin via hydrolyzation,acetylation,cyclic carbonatation,oxidation,decarbonatation,acylation,cyclic carbamatation and cyclization.

方法以克拉霉素为起始原料,经水解、乙酰化、环碳酸酯化、氧化、脱碳酸酯化、酰化、环氨基甲酸酯化和环合等反应合成目标化合物。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏酰基化反应引入乙酰基，接着溴化、胺化，得到标题树脂。该法避免了使氯甲醚。

Acylation activity of hydroxyl groups in methyl cholicate has been determined by the use of methacryloyl chloride, methacryloyl anhydride and methacrylic acid as the acylating agents.

以甲基丙烯酰氯、甲基丙烯酸酐和甲基丙烯酸酰化剂，研究了胆酸甲酯分子中羟基的反应活性。

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

方法以无水哌嗪为起始料,经酰、、胺、成等反应酸特拉唑嗪。

The chemical modification methods of food proteins are summarized,including acylation,deamidation,phosphorylation,glycosylation,covalent cross-linking effect etc.

综述了酰作用、去酰胺作用、磷酸作用、糖基作用、共价交联作用等食品蛋白质的学改性技术及方法。

Method The target compound was synthesized from clarithromycin via hydrolyzation,acetylation,cyclic carbonatation,oxidation,decarbonatation,acylation,cyclic carbamatation and cyclization.

方法以克拉霉素为起始料,经水解、乙酰、环碳酸酯、氧、脱碳酸酯、酰、环氨基甲酸酯和环合等反应合成目标合物。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏酰基反应引入乙酰基，接着溴、胺，到标题树脂。该法避免了使用氯甲醚。

Acylation activity of hydroxyl groups in methyl cholicate has been determined by the use of methacryloyl chloride, methacryloyl anhydride and methacrylic acid as the acylating agents.

以甲基丙烯酰氯、甲基丙烯酸酐和甲基丙烯酸作酰剂，研究了胆酸甲酯分子中羟基的反应活性。

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

方法以无水哌嗪为起,经酰化、还、胺化、成等反应制得酸特拉唑嗪。

The chemical modification methods of food proteins are summarized,including acylation,deamidation,phosphorylation,glycosylation,covalent cross-linking effect etc.

综述了酰化作用、去酰胺作用、磷酸化作用、糖基化作用、共价交作用等食品蛋白质的化学改性技术及方法。

Method The target compound was synthesized from clarithromycin via hydrolyzation,acetylation,cyclic carbonatation,oxidation,decarbonatation,acylation,cyclic carbamatation and cyclization.

方法以克拉霉素为起,经水解、乙酰化、环碳酸酯化、氧化、脱碳酸酯化、酰化、环氨基甲酸酯化和环合等反应合成目标化合物。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏酰基化反应引入乙酰基，接着溴化、胺化，得到标题树脂。该法避免了使用氯甲醚。

Acylation activity of hydroxyl groups in methyl cholicate has been determined by the use of methacryloyl chloride, methacryloyl anhydride and methacrylic acid as the acylating agents.

以甲基丙烯酰氯、甲基丙烯酸酐和甲基丙烯酸作酰化剂，研究了胆酸甲酯分子中羟基的反应活性。

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

方法以无水哌嗪原料,经酰化、还原、胺化、成等反应制得酸特拉唑嗪。

The chemical modification methods of food proteins are summarized,including acylation,deamidation,phosphorylation,glycosylation,covalent cross-linking effect etc.

综述了酰化作用、去酰胺作用、磷酸化作用、糖基化作用、共价交联作用等食品蛋白质的化学改性技术及方法。

Method The target compound was synthesized from clarithromycin via hydrolyzation,acetylation,cyclic carbonatation,oxidation,decarbonatation,acylation,cyclic carbamatation and cyclization.

方法以克拉霉素原料,经水解、乙酰化、环碳酸酯化、氧化、脱碳酸酯化、酰化、环氨基甲酸酯化和环合等反应合成目标化合物。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏酰基化反应引入乙酰基，接着溴化、胺化，得到标题树脂。该法避免了使用氯甲醚。

Acylation activity of hydroxyl groups in methyl cholicate has been determined by the use of methacryloyl chloride, methacryloyl anhydride and methacrylic acid as the acylating agents.

以甲基丙烯酰氯、甲基丙烯酸酐和甲基丙烯酸作酰化剂，研究了胆酸甲酯分子中羟基的反应活性。

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

方法以无水哌嗪为起始原料,经酰化、还原、胺化、成等反应制得特拉唑嗪。

The chemical modification methods of food proteins are summarized,including acylation,deamidation,phosphorylation,glycosylation,covalent cross-linking effect etc.

综述了酰化作用、去酰胺作用、磷化作用、糖基化作用、共价交联作用等食品蛋白质的化学改性技术及方法。

Method The target compound was synthesized from clarithromycin via hydrolyzation,acetylation,cyclic carbonatation,oxidation,decarbonatation,acylation,cyclic carbamatation and cyclization.

方法以克拉霉素为起始原料,经水解、乙酰化、环化、氧化、脱化、酰化、环氨基甲化和环合等反应合成目标化合物。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏酰基化反应引入乙酰基，接着溴化、胺化，得到标题树脂。该法避免了使用氯甲醚。

Acylation activity of hydroxyl groups in methyl cholicate has been determined by the use of methacryloyl chloride, methacryloyl anhydride and methacrylic acid as the acylating agents.

以甲基丙烯酰氯、甲基丙烯酐和甲基丙烯作酰化剂，研究了胆甲分子中羟基的反应活性。

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

法以无水哌嗪为起始原料,经化、还原、化、成等反应制得酸特拉唑嗪。

The chemical modification methods of food proteins are summarized,including acylation,deamidation,phosphorylation,glycosylation,covalent cross-linking effect etc.

综述了化作用、作用、磷酸化作用、糖基化作用、共价交联作用等食品蛋白质的化学改性技术及法。

Method The target compound was synthesized from clarithromycin via hydrolyzation,acetylation,cyclic carbonatation,oxidation,decarbonatation,acylation,cyclic carbamatation and cyclization.

法以克拉霉素为起始原料,经水解、乙化、环碳酸酯化、氧化、脱碳酸酯化、化、环氨基甲酸酯化和环合等反应合成目标化合物。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏基化反应引入乙基，接着溴化、化，得到标题树脂。该法避免了使用氯甲醚。

Acylation activity of hydroxyl groups in methyl cholicate has been determined by the use of methacryloyl chloride, methacryloyl anhydride and methacrylic acid as the acylating agents.

以甲基丙烯氯、甲基丙烯酸酐和甲基丙烯酸作化剂，研究了胆酸甲酯分子中羟基的反应活性。

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

方法以无水哌嗪为起始原料,经酰化、还原、化、成等反应制得酸特拉唑嗪。

The chemical modification methods of food proteins are summarized,including acylation,deamidation,phosphorylation,glycosylation,covalent cross-linking effect etc.

综述了酰化、去酰、磷酸化、糖基化、共价交联等食品蛋白质的化学改性技术及方法。

Method The target compound was synthesized from clarithromycin via hydrolyzation,acetylation,cyclic carbonatation,oxidation,decarbonatation,acylation,cyclic carbamatation and cyclization.

方法以克拉霉素为起始原料,经水解、乙酰化、环碳酸酯化、氧化、脱碳酸酯化、酰化、环氨基甲酸酯化和环合等反应合成目标化合物。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏酰基化反应引入乙酰基，接着溴化、化，得到标题树脂。该法避免了使氯甲醚。

Acylation activity of hydroxyl groups in methyl cholicate has been determined by the use of methacryloyl chloride, methacryloyl anhydride and methacrylic acid as the acylating agents.

以甲基丙烯酰氯、甲基丙烯酸酐和甲基丙烯酸酰化剂，研究了胆酸甲酯分子中羟基的反应活性。