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SYNTHESIS OF BORON TRIFLUORIDE COORDINATED COMPOUND AND OLIGONUCLEOTIDE

机译:氟化硼配位化合物和寡核苷酸的合成

摘要

PURPOSE: To obtain a new coordinated compound having an activity as a reaction accelerator in a phosphoramidite method higher than 1H-tetrazole, large solubility in an organic solvent, and combinedly having profitability and simplicity. ;CONSTITUTION: A boron trifluoride-benzimidazole complex of the formula is obtained by reacting (A) an ether complex obtained by dissolving boron trifluoride in an ether such as diethyl ether or tetrahydrofuran at room temperature with (B) benzimidazole in (C) a halogenated alkane solvent such as dichloromethane, chloroform, carbon tetrachloride or 1,2-dichloroethane in a molar ratio of A:B=1:1. The second objective oligonucleotide is obtained by reacting nucleoside phosphoramidite or nucleoside phosphonoamidite with nucleoside in the presence of the complex.;COPYRIGHT: (C)1996,JPO
机译:用途:获得一种新的配位化合物,该化合物在亚磷酰胺方法中具有比1H-四唑更高的作为反应促进剂的活性,在有机溶剂中的溶解度大,并且兼具盈利性和简便性。 ;组成:下式的三氟化硼-苯并咪唑配合物是通过使(A)在室温下将三氟化硼溶解在乙醚如四氢呋喃中的醚配合物与(B)苯并咪唑在(C)中的卤化反应而制得的烷烃溶剂,例如二氯甲烷,氯仿,四氯化碳或1,2-二氯乙烷,摩尔比为A:B = 1:1。第二个目的寡核苷酸是在复合物存在下,使核苷亚磷酰胺或核苷亚磷酰胺与核苷反应制得的。版权所有:(C)1996,日本特许厅

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