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

综述了二碘钐在分子内环反应中的应用。

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

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

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

方法克拉霉素为始原料,经水解、乙酰、环碳酸酯、氧、脱碳酸酯、酰、环氨基酸酯和环等反应成目标

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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.

邻氯酸和对乙氧基胺为原料,经过胺的、二芳胺的环、N-烷基、硫代反应成了N-丁基-2-乙氧基硫代吖啶酮。

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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基异唑3酰胺工艺的改进。

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

酐和取代为原料,经过乙酰、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。

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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的方法。

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