NaI/NPh3或NaI/PPh3在水中介导的β-二羰基化合物的可见光驱动α-羟基化反应

IF 4.7 1区 化学 Q1 CHEMISTRY, ORGANIC
Yan Wang, Zhongjie Wang, Hui Luo, Guohui Wang, Zhendong Shi, Yinfeng Ma, Jianglong Wu, Dianjun Li and Jinhui Yang
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引用次数: 0

摘要

通过水相中的电子供体-受体(EDA)复合物系统合成α-羟基羰基化合物的方法此前尚未见报道。本报告介绍了一种新型高效的 EDA 复合物系统,该系统采用了不需要事先安装的 β-二羰基底物、NaI 和廉价的 NPh3。构建这种 EDA 复合物的目的是改进和推进水相中的 EDA 光催化系统,同时保持对氧气的耐受性。以水为溶剂和氧气源,在非均相体系中利用该配合物实现了 β-二羰基衍生物的氢进化反应和水合羟化反应。该反应具有广泛的底物兼容性,无需相转移催化剂或额外的氧化剂,无碱、无金属,以及微反应器克级制备。该反应不仅适用于液体基质,而且当光传递受到不溶性固体基质的阻碍时,还可以通过提高绿色溶剂乙醇的浓度来达到理想的产率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Visible-light-driven α-hydroxylation of β-dicarbonyl compounds mediated by NaI/NPh3 or NaI/PPh3 in water†

Visible-light-driven α-hydroxylation of β-dicarbonyl compounds mediated by NaI/NPh3 or NaI/PPh3 in water†

The synthesis of α-hydroxy carbonyl compounds through the electron donor–acceptor (EDA) complex system in an aqueous phase has not been reported previously. This report presents a novel and efficient EDA complex system employing β-dicarbonyl substrates that do not require previous installation, NaI and inexpensive NPh3. The purpose of constructing this EDA complex is to improve and advance the EDA photocatalytic system in the aqueous phase, while maintaining tolerance to oxygen. The complexes were used to realize the hydrogen evolution reaction and hydration–hydroxylation of β-dicarbonyl derivatives in a non-homogeneous system using water as the solvent and oxygen source. The reaction exhibits broad substrate compatibility, does not need phase-transfer catalysts or additional oxidants, is alkali-free and metal-free, and allows microreactor gram-scale preparation. The reaction not only is suitable for liquid matrices but also can achieve the desired yield through an increase in the concentration of the green solvent ethanol, when the light transfer is obstructed by insoluble solid matrices.

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来源期刊
Organic Chemistry Frontiers
Organic Chemistry Frontiers CHEMISTRY, ORGANIC-
CiteScore
7.90
自引率
11.10%
发文量
686
审稿时长
1 months
期刊介绍: Organic Chemistry Frontiers is an esteemed journal that publishes high-quality research across the field of organic chemistry. It places a significant emphasis on studies that contribute substantially to the field by introducing new or significantly improved protocols and methodologies. The journal covers a wide array of topics which include, but are not limited to, organic synthesis, the development of synthetic methodologies, catalysis, natural products, functional organic materials, supramolecular and macromolecular chemistry, as well as physical and computational organic chemistry.
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