Photochemical tandem reaction of nitrogen containing heterocycles, bicyclo[1.1.1]pentane, and difluoroiodane(iii) reagents†

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Yaqing Zhu , Fengchao Yi , Ningning Zhou , Yi Zhang , Ying Zhang , Xia Zhao , Kui Lu
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引用次数: 0

Abstract

A visible light-induced difluoroalkylation/heteroarylation of [1.1.1]propellane with nitrogen containing heterocycles and difluoroiodane(iii) reagents was achieved. Various heteroarenes and difluoroiodane(iii) reagents exhibited good compatibility, yielding the desired products in moderate to good yields. The accessibility of the reagents and the mild reaction conditions establish this method as an alternative and practical strategy for accessing diverse 1-difluoroalkyl-3-heteroaryl bicyclo[1.1.1]pentanes (BCPs).

Abstract Image

含氮杂环、双环[1.1.1]戊烷和二氟碘烷(III)试剂的光化学串联反应。
利用含氮杂环和二氟碘烷(III)试剂实现了可见光诱导的[1.1.1]丙烷二氟烷基化/异芳基化反应。各种杂环和二氟碘烷(III)试剂表现出良好的兼容性,以中等至良好的产率获得所需的产物。试剂的易获得性和温和的反应条件使该方法成为获得多种 1-二氟烷基-3-杂芳基双环[1.1.1]戊烷(BCPs)的一种替代性实用策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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