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封面介绍The recent progress in the synthesis of α-tertiary amines via radical strategies is reviewed by Fang, Tian, Chen and Liu on page 22. Given the importance of α-tertiary amines and the advantages of radical reactions, various methods have been developed, including radical amina-tion/hydroamination of alkenes, radical C—N cross- coupling, radical addition of imines, and C—H bond activation of alkanes. -
封面介绍In recent years, f-block metal arene complexes with various structural features have been synthesized and characterized by Deng, Wang and Huang on page 56. Particularly, low-valent f-block metals can form δ- symmetry interactions with arenes, enabling the access of unusual oxidation states and unprecedented redox chemistry. This review surveys the recent advancement of f-block metal-arene interactions and provides an outlook on the future development. -
封面介绍The synthesis of novel near-infrared aggregation-indu- ced emission (AIE) molecules 1～3 by coupling two tri- arylamine-modified benzothiadiazole donnor-acceptor (D-A) units is reported by Dong, Su, Pan, Ren and Chen on page 205. In THF/H2O mixed solvents, the com-pounds 1～3 exhibited AIE properties with emission bands between 600～1000 nm and fluorescence quantum yields up to 13%. -
封面介绍As typical poly-fluorinated molecules, the α-trifluoro- methyl ketones are stable and useful compounds in or-ganic synthesis. For the sake of displaying the value of these compounds, the research advances on the synthesis of α-trifluoromethyl ketones, as well as the defluorina-tion-based synthetic application of these compounds for the synthesis of diverse other organic products are re-viewed by Cao, Liu and Wan on page 86.
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本期栏目
目录
综述与进展
有机化学
2025, 45 (1), pp 1-21
DOI: 10.6023/cjoc202407043
有机化学
2025, 45 (1), pp 22-41
DOI: 10.6023/cjoc202406040
有机化学
2025, 45 (1), pp 42-55
DOI: 10.6023/cjoc202407048
有机化学
2025, 45 (1), pp 56-85
DOI: 10.6023/cjoc202405017
有机化学
2025, 45 (1), pp 86-103
DOI: 10.6023/cjoc202411018
有机化学
2025, 45 (1), pp 104-135
DOI: 10.6023/cjoc202406043
有机化学
2025, 45 (1), pp 136-150
DOI: 10.6023/cjoc202406019
有机化学
2025, 45 (1), pp 151-167
DOI: 10.6023/cjoc202406007
有机化学
2025, 45 (1), pp 168-188
DOI: 10.6023/cjoc202404040
研究论文
有机化学
2025, 45 (1), pp 189-195
DOI: 10.6023/cjoc202410007
有机化学
2025, 45 (1), pp 196-204
DOI: 10.6023/cjoc202407021
有机化学
2025, 45 (1), pp 205-211
DOI: 10.6023/cjoc202407014
有机化学
2025, 45 (1), pp 212-219
DOI: 10.6023/cjoc202406008
有机化学
2025, 45 (1), pp 220-226
DOI: 10.6023/cjoc202406006
有机化学
2025, 45 (1), pp 227-239
DOI: 10.6023/cjoc202405024
有机化学
2025, 45 (1), pp 240-245
DOI: 10.6023/cjoc202405007
有机化学
2025, 45 (1), pp 246-255
DOI: 10.6023/cjoc202406010
有机化学
2025, 45 (1), pp 256-266
DOI: 10.6023/cjoc202406027
有机化学
2025, 45 (1), pp 267-275
DOI: 10.6023/cjoc202406005
有机化学
2025, 45 (1), pp 276-285
DOI: 10.6023/cjoc202405010
有机化学
2025, 45 (1), pp 286-296
DOI: 10.6023/cjoc202403053
有机化学
2025, 45 (1), pp 297-306
DOI: 10.6023/cjoc202406034
有机化学
2025, 45 (1), pp 307-318
DOI: 10.6023/cjoc202405027
有机化学
2025, 45 (1), pp 319-324
DOI: 10.6023/cjoc202407011
有机化学
2025, 45 (1), pp 325-330
DOI: 10.6023/cjoc202406004
有机化学
2025, 45 (1), pp 331-342
DOI: 10.6023/cjoc202405011
有机化学
2025, 45 (1), pp 343-348
DOI: 10.6023/cjoc202404042
有机化学
2025, 45 (1), pp 349-357
DOI: 10.6023/cjoc202404031
研究简报
有机化学
2025, 45 (1), pp 358-366
DOI: 10.6023/cjoc202405035
亮点述评
有机化学
2025, 45 (1), pp 367-369
DOI: 10.6023/cjoc202500001
有机化学
2025, 45 (1), pp 370-373
DOI: 10.6023/cjoc202500002
有机化学
2025, 45 (1), pp 374-375
DOI: 10.6023/cjoc202500003
