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

综述了二碘化钐在分子内环化应中的应用。

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,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应合成目标化合物。

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,酰化,还原,环合等应合成左西利嗪盐酸盐,应总收率为8.05%。

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,过乙酰化、解及环合应,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。

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为原,过克莱森缩合、环合、氨解应合成5甲基异唑3甲酰胺工艺的改进。

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,过胺的苯基化、二芳胺的环化、N-烷基化、硫代化应合成了N-丁基-2-乙氧基硫代吖啶酮。

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应,提供了一个方便地合成取代喹喔啉类化合物的方法。