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Synthesis of Tritium-Labeled Non-Natural Analogs of Purine and Pyrimidine Nucleosides
Radiochemistry ( IF 0.9 ) Pub Date : 2020-05-12 , DOI: 10.1134/s1066362220020149 G. V. Sidorov , N. F. Myasoedov
中文翻译:
Pur标记的嘌呤和嘧啶核苷的非天然类似物的合成
更新日期:2020-05-12
Radiochemistry ( IF 0.9 ) Pub Date : 2020-05-12 , DOI: 10.1134/s1066362220020149 G. V. Sidorov , N. F. Myasoedov
Abstract
Convenient preparative ways to synthesize tritium-labeled non-natural derivatives containing the cytosine and guanine moieties have been developed. The main distinction of these compounds from those already known consists in that they contain a chiral center. The tritium-labeled 2'-desoxy-3'-oxacytidine can was synthesized by the reaction of catalytic dehalogenation in solution of the corresponding 5-bromine-substituted compound; for 6-aminocyclopropyl-2'-desoxy-3'-oxaguanosine, the reaction of catalytic heterogeneous catalytic exchange in solution was used; for rest of compounds, the reaction of solid-phase catalytic hydrogenation (SCH) was employed.中文翻译:
Pur标记的嘌呤和嘧啶核苷的非天然类似物的合成