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通过 Ag(I)-催化的亲核试剂对 9-烯丙基-9H-嘌呤的加成反应构建无环核苷的新策略。

A new strategy to construct acyclic nucleosides via Ag(I)-catalyzed addition of pronucleophiles to 9-allenyl-9H-purines.

机构信息

Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, School of Chemistry and Chemical Engineering, Henan Normal University , Xinxiang, Henan 453007, P. R. China.

出版信息

Org Lett. 2014 Feb 7;16(3):900-3. doi: 10.1021/ol4036566. Epub 2014 Jan 17.

DOI:10.1021/ol4036566
PMID:24437554
Abstract

A new strategy to construct acyclic nucleosides with diverse side chains was developed. With Ag(I) salts as catalysts, the hydrocarboxylation, hydroamination, and hydrocarbonation reactions proceeded well, affording acyclic nucleosides in good yields (41 examples, 60-98% yields). Meanwhile, these reactions exhibited high chemoselectivities and E-selectivities.

摘要

开发了一种构建具有不同侧链的无环核苷的新策略。在 Ag(I)盐作为催化剂的条件下,氢羧化、氢氨化和氢化反应顺利进行,以良好的收率(41 个实例,60-98%的收率)得到了无环核苷。同时,这些反应表现出高化学选择性和 E-选择性。

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