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封面介绍An efficient visible-light induced nickel-catalyzed re-ductive Heck reaction of aryl halides and electron-defi-cient alkenes was developed by Liu, Zhao, Hu, Wang and Yuan on page 1691. Hantzsch ester was identified as a potent and very mild organic reductant to replace highly sensitive metal reductants in reductive Heck reaction. This reaction features mild reaction condition, broad substrate scope, and good functional group compatibility, thus providing an alternative approach for hydroarylation of alkenes. -
封面介绍The photocatalytic systems for converting biomass derivatives into value-added chemicals are summaried by Tan, Shi, Zhang and Li on page 1523. It categorizes homogeneous catalytic mechanisms (LMCT, PCET, HAT, SET) and the catalytic materials of TiO2, CdS, etc. in heterogenous catalysis, emphasizing their roles in activating C—C and C—O bonds via radical-mediated pathways. This work provides a strategic foundation for the complete depolymerization of lignin, enabling the green and efficient production of high-value aromatic compounds from recalcitrant biomass feedstocks. -
封面介绍The efficient transfer of nitrogen atom from ammonia and its equivalents to diverse organic compounds repre-sents the transfer of nitrogen from inorganic compounds to organic compounds resulting from the fixation of nitrogen gas. Therefore, it is of great value to develop the C—N bonding reaction involving ammonia and its equivalents by photocatalysis. The progress of light-catalyzed carbon-nitrogen bond-forming reactions invo-lving ammonia and its equivalents over recent years is summarized by Li, You, Li and Shu on page 1460. -
封面介绍The recent progress in hydrogen atom transfer-mediated photocatalytic C(sp3)—H bond oxidation achieved over the past five years is summarized by Huang, Huang and Hu on page 1509. The reaction mechanisms are ana-lyzed and the substrate scope of these photocatalytic systems is evaluated. Furthermore, prospect for future research directions in the rapidly developing field of photochemical C—H bond oxidation is proposed.
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本期栏目
目录
综述与进展
有机化学
2025, 45 (5), pp 1423-1459
DOI: 10.6023/cjoc202408003
有机化学
2025, 45 (5), pp 1460-1477
DOI: 10.6023/cjoc202405038
有机化学
2025, 45 (5), pp 1478-1508
DOI: 10.6023/cjoc202408025
有机化学
2025, 45 (5), pp 1509-1522
DOI: 10.6023/cjoc202409016
有机化学
2025, 45 (5), pp 1523-1547
DOI: 10.6023/cjoc202408018
有机化学
2025, 45 (5), pp 1548-1568
DOI: 10.6023/cjoc202408001
有机化学
2025, 45 (5), pp 1569-1590
DOI: 10.6023/cjoc202407049
有机化学
2025, 45 (5), pp 1591-1613
DOI: 10.6023/cjoc202407042
有机化学
2025, 45 (5), pp 1614-1633
DOI: 10.6023/cjoc202408004
有机化学
2025, 45 (5), pp 1634-1643
DOI: 10.6023/cjoc202408009
有机化学
2025, 45 (5), pp 1644-1668
DOI: 10.6023/cjoc202406018
有机化学
2025, 45 (5), pp 1669-1683
DOI: 10.6023/cjoc202405022
研究论文
有机化学
2025, 45 (5), pp 1684-1690
DOI: 10.6023/cjoc202409002
有机化学
2025, 45 (5), pp 1691-1697
DOI: 10.6023/cjoc202408039
有机化学
2025, 45 (5), pp 1698-1706
DOI: 10.6023/cjoc202407023
有机化学
2025, 45 (5), pp 1707-1715
DOI: 10.6023/cjoc202407036
有机化学
2025, 45 (5), pp 1716-1728
DOI: 10.6023/cjoc202407045
有机化学
2025, 45 (5), pp 1729-1738
DOI: 10.6023/cjoc202407040
有机化学
2025, 45 (5), pp 1739-1746
DOI: 10.6023/cjoc202407031
有机化学
2025, 45 (5), pp 1747-1754
DOI: 10.6023/cjoc202407010
有机化学
2025, 45 (5), pp 1755-1762
DOI: 10.6023/cjoc202406015
有机化学
2025, 45 (5), pp 1763-1769
DOI: 10.6023/cjoc202406003
有机化学
2025, 45 (5), pp 1770-1777
DOI: 10.6023/cjoc202403008
亮点述评
有机化学
2025, 45 (5), pp 1778-1780
DOI: 10.6023/cjoc202500012
有机化学
2025, 45 (5), pp 1781-1783
DOI: 10.6023/cjoc202500013
