Palladium-Catalyzed Transfer Iodination from Aryl Iodides to Nonactivated C(sp3)–H Bonds

IF 15.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Emilien Le Saux,  and , Bill Morandi*, 
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引用次数: 0

Abstract

We report a new strategy for the catalytic iodination of nonactivated C(sp3)–H bonds. The method merges the concepts of shuttle and light-enabled palladium catalysis to employ aryl iodides as both hydrogen atom transfer reagents and iodine donors. A noncanonical Pd0/PdI catalytic cycle is harnessed to transfer iodine from a C(sp2) to a C(sp3)–H bond under mild conditions, which tolerate sensitive functional groups. This mechanism is also applied to implement a C(sp3)–H thiolation that exploits reversible steps of the system.

Abstract Image

钯催化芳基碘化物向非活化C(sp3) -H键转移碘化
我们报道了一种催化碘化非活化C(sp3) -H键的新策略。该方法融合了穿梭和光钯催化的概念,采用芳基碘化物作为氢原子转移试剂和碘供体。利用非规范的Pd0/PdI催化循环,在温和条件下将碘从C(sp2)转移到C(sp3) -氢键上,可以耐受敏感官能团。该机制也被应用于实现C(sp3) -H巯基化,利用系统的可逆步骤。
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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