Photocatalytic C–C bond thio(seleno)esterification of 1,2-diketone-derived pro-aromatic intermediates†

IF 4.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chemical Communications Pub Date : 2025-02-28 DOI:10.1039/d4cc06735e
Amit Pal , Sudip Sarkar , Aaron Shibu , Prakash Maity , Basudev Sahoo
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Abstract

We report an organophotocatalyst-enabled oxidant-free C–S/C–Se bond coupling of (un)symmetrical 1,2-diketones via pro-aromatic dihydroquinazolinones/benzothiazolines, employing readily accessible disulfides/diselenides. In this scalable and redox-neutral method, various dialkyl, di(hetero)aryl, and alkyl-aryl 1,2-diketones are expediently converted to S-aryl (S-alkyl) alkyl/(hetero)aryl thioesters and Se-alkyl aryl selenoesters with broad functional group compatibility in high efficiency.

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光催化 C-C 键硫代(硒代)酯化 1,2-二酮衍生的原芳香族中间体。
我们报道了一种有机光催化剂激活的(非)对称1,2-二酮的无氧化剂C-S/C-Se键偶联,通过亲芳二氢喹唑啉酮/苯并噻唑啉,利用容易获得的二硫化物/二硒化物。在这种可扩展和氧化还原中性的方法中,各种二烷基、二(杂)芳基和烷基芳基1,2-二酮可以高效地转化为s -芳基(s -烷基)烷基/(杂)芳基硫酯和se -烷基芳基硒酸酯,具有广泛的官能团相容性。
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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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