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Extension of the 5-alkynyluridine side chain via C-C-bond formation in modified organometallic nucleosides using the Nicholas reaction.
Beilstein Journal of Organic Chemistry ( IF 2.7 ) Pub Date : 2020-01-02 , DOI: 10.3762/bjoc.16.1
Renata Kaczmarek 1 , Dariusz Korczyński 1 , James R Green 2 , Roman Dembinski 1, 3
Affiliation  

Dicobalt hexacarbonyl nucleoside complexes of propargyl ether or esters of 5-substituted uridines react with diverse C-nucleophiles. Synthetic outcomes confirmed that the Nicholas reaction can be carried out in a nucleoside presence, leading to a divergent synthesis of novel metallo-nucleosides enriched with alkene, arene, arylketo, and heterocyclic functions, in the deoxy and ribo series.

中文翻译:

使用Nicholas反应在修饰的有机金属核苷中通过CC键形成5-炔基尿苷侧链的延伸。

炔丙基醚或5-取代的尿苷的酯的二钴六羰基核苷络合物与各种C-亲核试剂反应。合成结果证实,尼古拉斯反应可在核苷存在下进行,从而导致脱氧和核糖系列中富含烯烃,芳烃,芳基酮和杂环功能的新型金属核苷的发散合成。
更新日期:2020-01-02
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