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封面介绍A novel electrochemical synthetic system for β-keto sulfonyl fluorides has been successfully developed by Feng, He, Li, Li, and Huang on page 3885. β-Keto sul-fonyl fluorides were synthesized using vinyl acetate and sulfuryl chlorofluoride under electrochemical conditions. The electroreductive strategy requires neither sacrificial electrodes nor metal catalysts, thus featuring mild conditions and a wide substrate scope, which enables the synthesis of various β-keto sulfonyl fluorides from sim-ple ketone feedstocks. Moreover, this transformation can be performed in a continuous flow reactor -
封面介绍A direct nitration of tertiary enamide with tert-butyl nitrite (tBuONO) under metal-free conditions is disclosed by Liu, Xu, Wang, Liu, Chen, and Sun on page 3903. A wide array of cyclic and acyclic enamides was nitrated with commercially available nonmetallic reagents, which produced diverse valuable β-acylamino nitroalkenes in excellent yields. Furthermore, this protocol is operationally simple and exhibits broad substrate scope and good functional group compatibility. -
封面介绍The recent progress in radical arylation reaction with diaryliodonium salts is reviewed by Zhu, Jiao, Wei, Chen, and Mo on page 3672. Radical arylations induced by visible light or without photocatalysis were used to the construction of carbon-carbon and carbon-hetero- atom bonds, and successfully applied in the synthesis of arylated bioactive compounds. -
封面介绍Atropisomeric phosphines are crucial to asymmetric catalysis yet challenging to synthesize. An N-hetero-cyclic carbene catalyzed reaction between dialdehydes and arylboronic acids is reported by Huang, Lin, Li, Zhang, Wang, Gao, Gong, Li, and Liu on page 3847. Mechanistic studies have revealed that the reaction initially undergoes a desymmetrization process, followed by a kinetic resolution pathway, affording a series of axially chiral phosphorus compounds with high enantio- selectivity.
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本期栏目
综述与进展
有机化学
2025, 45 (10), pp 3495-3516
DOI: 10.6023/cjoc202506019
有机化学
2025, 45 (10), pp 3517-3533
DOI: 10.6023/cjoc202505025
有机化学
2025, 45 (10), pp 3534-3545
DOI: 10.6023/cjoc202506034
有机化学
2025, 45 (10), pp 3546-3586
DOI: 10.6023/cjoc202505018
有机化学
2025, 45 (10), pp 3587-3612
DOI: 10.6023/cjoc202506010
有机化学
2025, 45 (10), pp 3613-3623
DOI: 10.6023/cjoc202505008
有机化学
2025, 45 (10), pp 3624-3643
DOI: 10.6023/cjoc202502040
有机化学
2025, 45 (10), pp 3644-3654
DOI: 10.6023/cjoc202501014
有机化学
2025, 45 (10), pp 3655-3671
DOI: 10.6023/cjoc202502004
有机化学
2025, 45 (10), pp 3672-3690
DOI: 10.6023/cjoc202412026
有机化学
2025, 45 (10), pp 3691-3700
DOI: 10.6023/cjoc202501016
有机化学
2025, 45 (10), pp 3701-3718
DOI: 10.6023/cjoc202411019
有机化学
2025, 45 (10), pp 3719-3740
DOI: 10.6023/cjoc202410018
有机化学
2025, 45 (10), pp 3741-3754
DOI: 10.6023/cjoc202409034
有机化学
2025, 45 (10), pp 3755-3776
DOI: 10.6023/cjoc202407034
研究论文
有机化学
2025, 45 (10), pp 3777-3785
DOI: 10.6023/cjoc202506037
有机化学
2025, 45 (10), pp 3786-3796
DOI: 10.6023/cjoc202506004
有机化学
2025, 45 (10), pp 3797-3806
DOI: 10.6023/cjoc202504022
有机化学
2025, 45 (10), pp 3807-3815
DOI: 10.6023/cjoc202503018
有机化学
2025, 45 (10), pp 3816-3823
DOI: 10.6023/cjoc202503005
有机化学
2025, 45 (10), pp 3824-3837
DOI: 10.6023/cjoc202505007
有机化学
2025, 45 (10), pp 3838-3846
DOI: 10.6023/cjoc202502029
有机化学
2025, 45 (10), pp 3847-3855
DOI: 10.6023/cjoc202504014
有机化学
2025, 45 (10), pp 3856-3865
DOI: 10.6023/cjoc202503002
有机化学
2025, 45 (10), pp 3866-3872
DOI: 10.6023/cjoc202502030
有机化学
2025, 45 (10), pp 3873-3884
DOI: 10.6023/cjoc202502009
有机化学
2025, 45 (10), pp 3885-3891
DOI: 10.6023/cjoc202412021
有机化学
2025, 45 (10), pp 3892-3902
DOI: 10.6023/cjoc202412015
有机化学
2025, 45 (10), pp 3903-3911
DOI: 10.6023/cjoc202412011
有机化学
2025, 45 (10), pp 3912-3922
DOI: 10.6023/cjoc202410012
有机化学
2025, 45 (10), pp 3923-3931
DOI: 10.6023/cjoc202502039
亮点述评
有机化学
2025, 45 (10), pp 3931-3933
DOI: 10.6023/cjoc202500022
有机化学
2025, 45 (10), pp 3934-3935
DOI: 10.6023/cjoc202500023
