Application of samarium diiodide in mediating intramolecular cyclization reactions was reviewed.

综述了二碘化钐在分子内环化反应中的应用。

Levocetirizine Dihydrochloride was prepared from benzoyl chloride by acidylation,hydrogenation,cyclization with an overall yield of 8.05%.

以苯甲酰氯,酰化,还,环合等反应合成左旋西替利嗪盐酸盐,反应总收率8.05%。

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

方法以克拉霉素起始,水解、乙酰化、环酸酯化、氧化、脱酸酯化、酰化、环氨基甲酸酯化和环合等反应合成目标化合物。

N butyl 2 ethoxy thioacridone was prepared from o chloro benzoic acid and p phenetidine by means of Ullman reaction,cyclization,N alkylation and sulfurization.

以邻氯苯甲酸和对乙氧基苯胺,过胺的苯基化、二芳胺的环化、N-烷基化、硫代化反应合成了N-丁基-2-乙氧基硫代吖啶酮。

This paper reports the improvement on the synthesis of 5 methylisoxazol 3 formamide by Claisen condensation of diethyl oxalacetate followed by cyclization and ammonolysis.

讨论了以草酸二乙酯,过克莱森缩合、环合、氨解反应合成5甲基异唑3甲酰胺工艺的改进。

In this paper, the synthesis of 2 - chloranthraquinone and 2 - aminoanthraquinone was studied.It was prepared from phthalic anhydride by acetyiation, hydrolysis and cyclization.

以苯酐和取代苯,过乙酰化、水解及环合反应,合成了2-氯蒽醌和2-氨基蒽醌,并对影响收率的工艺条件进行了研究。

Aqueous titanium trichloride promoted intermolecular reductive cyclization of 1,2 -diketone and o-nitroaniline in basic media provides a convenient method for the synthesis of quinoxaline derivatives.

本文研究了三氯化钛水溶液作用下,邻硝基苯胺与1,2-二酮在碱性介质中分子间的成环反应,提供了一个方便地合成取代喹喔啉类化合物的方法。

Application of samarium diiodide in mediating intramolecular cyclization reactions was reviewed.

综述了钐在分子内环中的用。

Levocetirizine Dihydrochloride was prepared from benzoyl chloride by acidylation,hydrogenation,cyclization with an overall yield of 8.05%.

以苯甲酰氯为原料,经酰,还原,环等成左旋西替利嗪盐酸盐,总收率为8.05%。

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、环酸酯、氧、脱酸酯、酰、环氨基甲酸酯和环等成目标物。

N butyl 2 ethoxy thioacridone was prepared from o chloro benzoic acid and p phenetidine by means of Ullman reaction,cyclization,N alkylation and sulfurization.

以邻氯苯甲酸和对乙氧基苯胺为原料,经过胺的苯基、芳胺的环、N-烷基、硫代成了N-丁基-2-乙氧基硫代吖啶酮。

This paper reports the improvement on the synthesis of 5 methylisoxazol 3 formamide by Claisen condensation of diethyl oxalacetate followed by cyclization and ammonolysis.

讨论了以草酸乙酯为原料,经过克莱森缩、环、氨解成5甲基异唑3甲酰胺工艺的改进。

In this paper, the synthesis of 2 - chloranthraquinone and 2 - aminoanthraquinone was studied.It was prepared from phthalic anhydride by acetyiation, hydrolysis and cyclization.

以苯酐和取代苯为原料,经过乙酰、水解及环,成了2-氯蒽醌和2-氨基蒽醌,并对影响收率的工艺条件进行了研究。

Aqueous titanium trichloride promoted intermolecular reductive cyclization of 1,2 -diketone and o-nitroaniline in basic media provides a convenient method for the synthesis of quinoxaline derivatives.

本文研究了三氯钛水溶液作用下,邻硝基苯胺与1,2-酮在碱性介质中分子间的成环,提供了一个方便地成取代喹喔啉类物的方法。

Application of samarium diiodide in mediating intramolecular cyclization reactions was reviewed.

综述了二碘化钐在分子内环化反应中的应用。

Levocetirizine Dihydrochloride was prepared from benzoyl chloride by acidylation,hydrogenation,cyclization with an overall yield of 8.05%.

苯甲酰氯为原料,经酰化,还原,环等反应成左西利嗪盐酸盐,反应总收率为8.05%。

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

方法克拉霉素为起始原料,经水解、乙酰化、环酸酯化、氧化、脱酸酯化、酰化、环氨基甲酸酯化和环等反应成目标化。

N butyl 2 ethoxy thioacridone was prepared from o chloro benzoic acid and p phenetidine by means of Ullman reaction,cyclization,N alkylation and sulfurization.

邻氯苯甲酸和对乙氧基苯胺为原料,经过胺的苯基化、二芳胺的环化、N-烷基化、硫代化反应成了N-丁基-2-乙氧基硫代吖啶酮。

This paper reports the improvement on the synthesis of 5 methylisoxazol 3 formamide by Claisen condensation of diethyl oxalacetate followed by cyclization and ammonolysis.

讨论了草酸二乙酯为原料,经过克莱森缩、环、氨解反应成5甲基异唑3甲酰胺工艺的改进。

In this paper, the synthesis of 2 - chloranthraquinone and 2 - aminoanthraquinone was studied.It was prepared from phthalic anhydride by acetyiation, hydrolysis and cyclization.

苯酐和取代苯为原料,经过乙酰化、水解及环反应,成了2-氯蒽醌和2-氨基蒽醌,并对影响收率的工艺条件进行了研究。

Aqueous titanium trichloride promoted intermolecular reductive cyclization of 1,2 -diketone and o-nitroaniline in basic media provides a convenient method for the synthesis of quinoxaline derivatives.

本文研究了三氯化钛水溶液作用下,邻硝基苯胺与1,2-二酮在碱性介质中分子间的成环反应,提供了一个方便地成取代喹喔啉类化的方法。

Application of samarium diiodide in mediating intramolecular cyclization reactions was reviewed.

综述了二碘化钐在分子内环化反应中的应用。

Levocetirizine Dihydrochloride was prepared from benzoyl chloride by acidylation,hydrogenation,cyclization with an overall yield of 8.05%.

苯甲酰氯为原料,经酰化,还原,环合等反应合成左旋西替利嗪盐盐,反应总收率为8.05%。

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

方法克拉霉素为起始原料,经水解、乙酰化、环酯化、氧化、脱酯化、酰化、环氨基甲酯化和环合等反应合成目标化合物。

N butyl 2 ethoxy thioacridone was prepared from o chloro benzoic acid and p phenetidine by means of Ullman reaction,cyclization,N alkylation and sulfurization.

邻氯苯甲和对乙氧基苯胺为原料,经过胺的苯基化、二芳胺的环化、N-烷基化、硫代化反应合成了N-丁基-2-乙氧基硫代吖啶酮。

This paper reports the improvement on the synthesis of 5 methylisoxazol 3 formamide by Claisen condensation of diethyl oxalacetate followed by cyclization and ammonolysis.

讨论了二乙酯为原料,经过克莱森缩合、环合、氨解反应合成5甲基异唑3甲酰胺工艺的改进。

In this paper, the synthesis of 2 - chloranthraquinone and 2 - aminoanthraquinone was studied.It was prepared from phthalic anhydride by acetyiation, hydrolysis and cyclization.

苯酐和取代苯为原料,经过乙酰化、水解及环合反应,合成了2-氯蒽醌和2-氨基蒽醌,并对影响收率的工艺条件进行了研究。

Aqueous titanium trichloride promoted intermolecular reductive cyclization of 1,2 -diketone and o-nitroaniline in basic media provides a convenient method for the synthesis of quinoxaline derivatives.

本文研究了三氯化钛水溶液作用下,邻硝基苯胺与1,2-二酮在碱性介质中分子间的成环反应,提供了一个方便地合成取代喹喔啉类化合物的方法。

Application of samarium diiodide in mediating intramolecular cyclization reactions was reviewed.

综述了二碘化钐在分子内环化反应中的应用。

Levocetirizine Dihydrochloride was prepared from benzoyl chloride by acidylation,hydrogenation,cyclization with an overall yield of 8.05%.

苯甲酰氯为原料,经酰化,还原,环等反应成左西利嗪盐酸盐,反应总收率为8.05%。

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

方法克拉霉素为起始原料,经水解、乙酰化、环酸酯化、氧化、脱酸酯化、酰化、环氨基甲酸酯化和环等反应成目标化。

N butyl 2 ethoxy thioacridone was prepared from o chloro benzoic acid and p phenetidine by means of Ullman reaction,cyclization,N alkylation and sulfurization.

邻氯苯甲酸和对乙氧基苯胺为原料,经过胺的苯基化、二芳胺的环化、N-烷基化、硫代化反应成了N-丁基-2-乙氧基硫代吖啶酮。

This paper reports the improvement on the synthesis of 5 methylisoxazol 3 formamide by Claisen condensation of diethyl oxalacetate followed by cyclization and ammonolysis.

讨论了草酸二乙酯为原料,经过克莱森缩、环、氨解反应成5甲基异唑3甲酰胺工艺的改进。

In this paper, the synthesis of 2 - chloranthraquinone and 2 - aminoanthraquinone was studied.It was prepared from phthalic anhydride by acetyiation, hydrolysis and cyclization.

苯酐和取代苯为原料,经过乙酰化、水解及环反应,成了2-氯蒽醌和2-氨基蒽醌,并对影响收率的工艺条件进行了研究。

Aqueous titanium trichloride promoted intermolecular reductive cyclization of 1,2 -diketone and o-nitroaniline in basic media provides a convenient method for the synthesis of quinoxaline derivatives.

本文研究了三氯化钛水溶液作用下,邻硝基苯胺与1,2-二酮在碱性介质中分子间的成环反应,提供了一个方便地成取代喹喔啉类化的方法。

Application of samarium diiodide in mediating intramolecular cyclization reactions was reviewed.

综述了二碘化钐在分子内环化反应中的应用。

Levocetirizine Dihydrochloride was prepared from benzoyl chloride by acidylation,hydrogenation,cyclization with an overall yield of 8.05%.

以苯甲原料,化,还原,环合等反应合成左旋西替利嗪盐酸盐,反应总收率8.05%。

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

方法以克拉霉素起始原料,水解、乙化、环酸酯化、氧化、脱酸酯化、化、环氨基甲酸酯化和环合等反应合成目标化合物。

N butyl 2 ethoxy thioacridone was prepared from o chloro benzoic acid and p phenetidine by means of Ullman reaction,cyclization,N alkylation and sulfurization.

以邻苯甲酸和对乙氧基苯原料,的苯基化、二芳的环化、N-烷基化、硫代化反应合成了N-丁基-2-乙氧基硫代吖啶酮。

This paper reports the improvement on the synthesis of 5 methylisoxazol 3 formamide by Claisen condensation of diethyl oxalacetate followed by cyclization and ammonolysis.

讨论了以草酸二乙酯原料,克莱森缩合、环合、氨解反应合成5甲基异唑3甲工艺的改进。

In this paper, the synthesis of 2 - chloranthraquinone and 2 - aminoanthraquinone was studied.It was prepared from phthalic anhydride by acetyiation, hydrolysis and cyclization.

以苯酐和取代苯原料,乙化、水解及环合反应,合成了2-蒽醌和2-氨基蒽醌,并对影响收率的工艺条件进行了研究。

Aqueous titanium trichloride promoted intermolecular reductive cyclization of 1,2 -diketone and o-nitroaniline in basic media provides a convenient method for the synthesis of quinoxaline derivatives.

本文研究了三化钛水溶液作用下,邻硝基苯与1,2-二酮在碱性介质中分子间的成环反应,提供了一个方便地合成取代喹喔啉类化合物的方法。

Application of samarium diiodide in mediating intramolecular cyclization reactions was reviewed.

综述了二碘化钐在分子内环化反应中的应用。

Levocetirizine Dihydrochloride was prepared from benzoyl chloride by acidylation,hydrogenation,cyclization with an overall yield of 8.05%.

以苯甲酰氯为原料,经酰化,还原,环合等反应合成左旋西替利嗪盐酸盐,反应总收率为8.05%。

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、酰化、环酸酯化、化、脱酸酯化、酰化、环氨甲酸酯化和环合等反应合成目标化合物。

N butyl 2 ethoxy thioacridone was prepared from o chloro benzoic acid and p phenetidine by means of Ullman reaction,cyclization,N alkylation and sulfurization.

以邻氯苯甲酸和对苯胺为原料,经过胺的苯化、二芳胺的环化、N-烷化、硫代化反应合成了N-丁-2-硫代吖啶酮。

This paper reports the improvement on the synthesis of 5 methylisoxazol 3 formamide by Claisen condensation of diethyl oxalacetate followed by cyclization and ammonolysis.

讨论了以草酸二酯为原料,经过克莱森缩合、环合、氨解反应合成5甲异唑3甲酰胺工艺的改进。

In this paper, the synthesis of 2 - chloranthraquinone and 2 - aminoanthraquinone was studied.It was prepared from phthalic anhydride by acetyiation, hydrolysis and cyclization.

以苯酐和取代苯为原料,经过酰化、水解及环合反应,合成了2-氯蒽醌和2-氨蒽醌,并对影响收率的工艺条件进行了研究。

Aqueous titanium trichloride promoted intermolecular reductive cyclization of 1,2 -diketone and o-nitroaniline in basic media provides a convenient method for the synthesis of quinoxaline derivatives.

本文研究了三氯化钛水溶液作用下,邻硝苯胺与1,2-二酮在碱性介质中分子间的成环反应,提供了一个方便地合成取代喹喔啉类化合物的方法。

Application of samarium diiodide in mediating intramolecular cyclization reactions was reviewed.

综述了二碘化钐在分子内化反应中的应用。

Levocetirizine Dihydrochloride was prepared from benzoyl chloride by acidylation,hydrogenation,cyclization with an overall yield of 8.05%.

以苯甲酰氯为原料,经酰化,还原,反应成左旋西替利嗪盐酸盐,反应总收率为8.05%。

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、酰化、酸酯化、氧化、脱酸酯化、酰化、氨基甲酸酯化反应成目标化物。

N butyl 2 ethoxy thioacridone was prepared from o chloro benzoic acid and p phenetidine by means of Ullman reaction,cyclization,N alkylation and sulfurization.

以邻氯苯甲酸氧基苯胺为原料,经过胺的苯基化、二芳胺的化、N-烷基化、硫代化反应成了N-丁基-2-氧基硫代吖啶酮。

This paper reports the improvement on the synthesis of 5 methylisoxazol 3 formamide by Claisen condensation of diethyl oxalacetate followed by cyclization and ammonolysis.

讨论了以草酸二酯为原料,经过克莱森缩、、氨解反应成5甲基异唑3甲酰胺工艺的改进。

In this paper, the synthesis of 2 - chloranthraquinone and 2 - aminoanthraquinone was studied.It was prepared from phthalic anhydride by acetyiation, hydrolysis and cyclization.

以苯酐取代苯为原料,经过酰化、水解及反应,成了2-氯蒽醌2-氨基蒽醌,并影响收率的工艺条件进行了研究。

Aqueous titanium trichloride promoted intermolecular reductive cyclization of 1,2 -diketone and o-nitroaniline in basic media provides a convenient method for the synthesis of quinoxaline derivatives.

本文研究了三氯化钛水溶液作用下,邻硝基苯胺与1,2-二酮在碱性介质中分子间的成反应,提供了一个方便地成取代喹喔啉类化物的方法。

Application of samarium diiodide in mediating intramolecular cyclization reactions was reviewed.

综述了二碘化钐在分子内环化反应中的应用。

Levocetirizine Dihydrochloride was prepared from benzoyl chloride by acidylation,hydrogenation,cyclization with an overall yield of 8.05%.

以苯甲酰氯为原料,经酰化,还原,环合等反应合成左旋西替利嗪盐酸盐,反应总收率为8.05%。

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、酰化、环酸酯化、化、脱酸酯化、酰化、环氨甲酸酯化和环合等反应合成目标化合物。

N butyl 2 ethoxy thioacridone was prepared from o chloro benzoic acid and p phenetidine by means of Ullman reaction,cyclization,N alkylation and sulfurization.

以邻氯苯甲酸和对苯胺为原料,经过胺的苯化、二芳胺的环化、N-烷化、硫代化反应合成了N-丁-2-硫代吖啶酮。

This paper reports the improvement on the synthesis of 5 methylisoxazol 3 formamide by Claisen condensation of diethyl oxalacetate followed by cyclization and ammonolysis.

讨论了以草酸二酯为原料,经过克莱森缩合、环合、氨解反应合成5甲异唑3甲酰胺工艺的改进。

In this paper, the synthesis of 2 - chloranthraquinone and 2 - aminoanthraquinone was studied.It was prepared from phthalic anhydride by acetyiation, hydrolysis and cyclization.

以苯酐和取代苯为原料,经过酰化、水解及环合反应,合成了2-氯蒽醌和2-氨蒽醌,并对影响收率的工艺条件进行了研究。

Aqueous titanium trichloride promoted intermolecular reductive cyclization of 1,2 -diketone and o-nitroaniline in basic media provides a convenient method for the synthesis of quinoxaline derivatives.

本文研究了三氯化钛水溶液作用下,邻硝苯胺与1,2-二酮在碱性介质中分子间的成环反应,提供了一个方便地合成取代喹喔啉类化合物的方法。