Iron-catalyzed regioselective α,α-dichlorocarbonylation of alkynes under photo-irradiation

IF 1.5 4区 化学 Q3 CHEMISTRY, ORGANIC
Chen Bao, Meng Guan
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引用次数: 0

Abstract

α,α-Dichlorocarbonyl core exhibited unique versatility towards a series of cyclic and acyclic scaffolds. Besides, it is ubiquitous in numerous biologically interesting products. As such, efficient and divergent synthetic methodology for achieving α,α-dichlorocarbonyl structural core under mild conditions attracted tremendous attentions so far. In this paper, an efficient route for the synthesis of α,α-dichlorocarbonyl compounds via an oxidative nucleophilic oxychlorination of alkyne under iron/photo dual catalysis is described under mild conditions.

Abstract Image

光照射下铁催化区域选择性α,α-二氯羰基化反应
α,α-二氯羰基核对一系列环和非环支架具有独特的通用性。此外,它在许多生物有趣的产品中无处不在。因此,在温和条件下制备α,α-二氯羰基结构核的高效、多样化的合成方法备受关注。本文介绍了在温和条件下,铁/光双催化下,炔氧化亲核氯化反应合成α,α-二氯羰基化合物的有效途径。
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来源期刊
Tetrahedron Letters
Tetrahedron Letters 化学-有机化学
CiteScore
3.50
自引率
5.60%
发文量
521
审稿时长
28 days
期刊介绍: Tetrahedron Letters provides maximum dissemination of outstanding developments in organic chemistry. The journal is published weekly and covers developments in techniques, structures, methods and conclusions in experimental and theoretical organic chemistry. Rapid publication of timely and significant research results enables researchers from all over the world to transmit quickly their new contributions to large, international audiences.
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