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封面介绍An efficient copper-catalyzed asymmetric hydroboration of 1-benzoyl-2,3-dihydropyridin-4(1H)-ones is reported by Wu, Sun, and Xu on page 2816. This protocol features a broad substrate scope, tolerating various N-acyl substituents (aryl, naphthoyl, heteroaryl, pivaloyl) and substituted benzoyl moieties, affording cyclic α-aminoboronate esters with up to 99% yield and ee values of 84%～96%. A plausible mechanism invo- lving a borylcopper intermediate and σ-bond metathesis is proposed. -
封面介绍To realize earth-abundant nickel-catalyzed C(sp2)—N coupling of aryl halides with sulfonamide compounds under irradiation from 390～395 nm LEDs irradiation, a mild and efficient method that requires no external photosensitizer was developed by Wang, Liu, Song, Shi, and Xue on page 2835. The nickel-catalyzed protocol with soluble amine bases boasts easily accessible star- ting materials, mild reaction conditions, simple opera- tion, broad substrate scope, and excellent functional- group tolerance. -
封面介绍The recent advances over the past five years in cobalt- cata-lyzed C—S bond formation for the synthesis of various or-ganosulfur compounds are systematically summarized by Xiao and Zhong on page 2644. The advantages of cobalt as an earth-abundant, low-cost metal with variable oxidation states and low biotoxicity are highlighted, which enable efficient sulfurization under mild conditions with excellent chemoselectivity and functional group tolerance. -
封面介绍The α-branched methylation of ketones with methanol catalyzed by a bis-N-heterocyclic carbene manganese(I) complex under phosphine-free conditions was reported by Lan, Yu, Chen, Yang, Wang and Ke on page 2751. A broad range of aromatic propiophenone derivatives are well-tolerated and selective double methylation is also feasible for acetophenone derivatives with good product yields.
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本期栏目
目录
综述与进展
有机化学
2026, 46 (7), pp 2493-2510
DOI: 10.6023/cjoc202603032
有机化学
2026, 46 (7), pp 2511-2528
DOI: 10.6023/cjoc202602024
有机化学
2026, 46 (7), pp 2529-2543
DOI: 10.6023/cjoc202602023
有机化学
2026, 46 (7), pp 2544-2562
DOI: 10.6023/cjoc202603020
有机化学
2026, 46 (7), pp 2563-2580
DOI: 10.6023/cjoc202604003
有机化学
2026, 46 (7), pp 2581-2588
DOI: 10.6023/cjoc202604006
有机化学
2026, 46 (7), pp 2589-2603
DOI: 10.6023/cjoc202603047
有机化学
2026, 46 (7), pp 2604-2621
DOI: 10.6023/cjoc202602020
有机化学
2026, 46 (7), pp 2622-2643
DOI: 10.6023/cjoc202602021
有机化学
2026, 46 (7), pp 2644-2668
DOI: 10.6023/cjoc202603022
有机化学
2026, 46 (7), pp 2669-2682
DOI: 10.6023/cjoc202603006
有机化学
2026, 46 (7), pp 2683-2700
DOI: 10.6023/cjoc202601041
有机化学
2026, 46 (7), pp 2701-2712
DOI: 10.6023/cjoc202601004
研究论文
有机化学
2026, 46 (7), pp 2713-2722
DOI: 10.6023/cjoc202604052
有机化学
2026, 46 (7), pp 2723-2732
DOI: 10.6023/cjoc202603037
有机化学
2026, 46 (7), pp 2733-2742
DOI: 10.6023/cjoc202603002
有机化学
2026, 46 (7), pp 2743-2750
DOI: 10.6023/cjoc202603041
有机化学
2026, 46 (7), pp 2751-2759
DOI: 10.6023/cjoc202603028
有机化学
2026, 46 (7), pp 2760-2769
DOI: 10.6023/cjoc202603046
有机化学
2026, 46 (7), pp 2770-2778
DOI: 10.6023/cjoc202603035
有机化学
2026, 46 (7), pp 2779-2788
DOI: 10.6023/cjoc202603034
有机化学
2026, 46 (7), pp 2789-2795
DOI: 10.6023/cjoc202602003
有机化学
2026, 46 (7), pp 2796-2807
DOI: 10.6023/cjoc202602016
有机化学
2026, 46 (7), pp 2808-2815
DOI: 10.6023/cjoc202601010
有机化学
2026, 46 (7), pp 2816-2824
DOI: 10.6023/cjoc202602002
有机化学
2026, 46 (7), pp 2825-2834
DOI: 10.6023/cjoc202512045
有机化学
2026, 46 (7), pp 2835-2852
DOI: 10.6023/cjoc202511014
亮点述评
有机化学
2026, 46 (7), pp 2853-2855
DOI: 10.6023/cjoc202600012
有机化学
2026, 46 (7), pp 2856-2857
DOI: 10.6023/cjoc202600013
