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封面介绍Photocatalytic heterogeneous chlorotrifluoromethylation and iodoperfluoroalkylation of unactivated terminal alkenes achieved under the catalysis of PTH-POP (phe-nylphenothiazine-based porous organic polymer) are reported by Wang, Gao, Zhou and Zhang on page 1136. This method offers a transition-metal-free and recyclable platform to access valuable perfluoroalkylated compounds in a highly efficient fashion. -
封面介绍The catalytic asymmetric reactions involving o-hydroxy- benzyl alcohols, a kind of o-quinone methide precursors with unique advantages, are summarized by Wang, Yang, Zhang and Shi on page 974. This review will open a new window for the design of new kinds of o-hyd- roxybenzyl alcohols and their involved catalytic asym-metric reactions. Notably, this review is dedicated to the special issue “Women Scientists in China” to celebrate the International Women’s Day. -
封面介绍A light-promoted radical tandem cyclization reaction to synthesize difluoroalkylindoles was developed by Zhao, Wei, Ke, and Li on page 1102. By using difluorobromo- esters and 3-alkenyl indoles, varies of fluorine-contain- ing polycyclic indoles were generated in an easy-to- operate and mild in conditions with a wide range of substrate adaptability and good yields. -
封面介绍The reaction of transition metals catalyzed the activation of C(sp3)—H bonds to form carbon-nitrogen bonds has been a challenging and hot research area. Important progress has been made in directing group-assisted C(sp3)—H bond amination reactions, and many catalyst systems based on different transition metals with cheap and efficient amination reagents have been developed. The research progress of transition metal-catalyzed C(sp3)—H nitrene insertion reaction assisted by dire- cting groups in the past decade is reviewed by Yang, Liu, and Wang on page 914
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本期栏目
目录
综述与进展
有机化学
2023, 43 (3), pp 791-808
DOI: 10.6023/cjoc202211043
有机化学
2023, 43 (3), pp 809-825
DOI: 10.6023/cjoc202302015
有机化学
2023, 43 (3), pp 826-854
DOI: 10.6023/cjoc202211046
有机化学
2023, 43 (3), pp 855-872
DOI: 10.6023/cjoc202212039
有机化学
2023, 43 (3), pp 873-891
DOI: 10.6023/cjoc202301004
有机化学
2023, 43 (3), pp 892-913
DOI: 10.6023/cjoc202211049
有机化学
2023, 43 (3), pp 914-923
DOI: 10.6023/cjoc202211041
有机化学
2023, 43 (3), pp 924-948
DOI: 10.6023/cjoc202211039
有机化学
2023, 43 (3), pp 949-960
DOI: 10.6023/cjoc202301009
有机化学
2023, 43 (3), pp 961-973
DOI: 10.6023/cjoc202211045
有机化学
2023, 43 (3), pp 974-999
DOI: 10.6023/cjoc202211022
有机化学
2023, 43 (3), pp 1000-1011
DOI: 10.6023/cjoc202211042
有机化学
2023, 43 (3), pp 1012-1022
DOI: 10.6023/cjoc202211048
有机化学
2023, 43 (3), pp 1023-1035
DOI: 10.6023/cjoc202211032
有机化学
2023, 43 (3), pp 1036-1044
DOI: 10.6023/cjoc202211047
有机化学
2023, 43 (3), pp 1045-1068
DOI: 10.6023/cjoc202211040
有机化学
2023, 43 (3), pp 1069-1083
DOI: 10.6023/cjoc202210032
研究论文
有机化学
2023, 43 (3), pp 1084-1090
DOI: 10.6023/cjoc202301011
有机化学
2023, 43 (3), pp 1091-1101
DOI: 10.6023/cjoc202211028
有机化学
2023, 43 (3), pp 1102-1114
DOI: 10.6023/cjoc202212032
有机化学
2023, 43 (3), pp 1115-1123
DOI: 10.6023/cjoc202210033
有机化学
2023, 43 (3), pp 1124-1135
DOI: 10.6023/cjoc202211038
有机化学
2023, 43 (3), pp 1136-1145
DOI: 10.6023/cjoc202211013
有机化学
2023, 43 (3), pp 1146-1156
DOI: 10.6023/cjoc202210031
有机化学
2023, 43 (3), pp 1157-1167
DOI: 10.6023/cjoc202210009
有机化学
2023, 43 (3), pp 1168-1176
DOI: 10.6023/cjoc202209021
有机化学
2023, 43 (3), pp 1177-1186
DOI: 10.6023/cjoc202208034
有机化学
2023, 43 (3), pp 1187-1196
DOI: 10.6023/cjoc202206052
亮点述评
有机化学
2023, 43 (3), pp 1197-1198
DOI: 10.6023/cjoc202300011
有机化学
2023, 43 (3), pp 1199-1200
DOI: 10.6023/cjoc202300012
有机化学
2023, 43 (3), pp 1201-1202
DOI: 10.6023/cjoc202300013
有机化学
2023, 43 (3), pp 1203-1205
DOI: 10.6023/cjoc202300014
有机化学
2023, 43 (3), pp 1206-1207
DOI: 10.6023/cjoc202300015
有机化学
2023, 43 (3), pp 1208-1210
DOI: 10.6023/cjoc202300016
有机化学
2023, 43 (3), pp 1211-1212
DOI: 10.6023/cjoc202300017
有机化学
2023, 43 (3), pp 1213-1214
DOI: 10.6023/cjoc202300018
