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封面介绍In recent years, significant progress has been made in the enantioselective synthesis of P-chiral phosphine oxides, which are of importance in pharmaceuticals and asymmetric catalysis. The attractive achievements from 2020 to 2022 are summarized and discussed by Luo, Yin, and Jiang on page 1963. -
封面介绍The recent progress on the catalytic asymmetric synthesis of N—N atropisomers is reviewed by Song, Li, Huang, Jia, and Mei on page 1977. The N—N bond is widely found in natural products and bioactive compounds. The atropisomerism of N—N bond, however, had been dismissed for a long time due to the stereotype that N—N axis is unstable. Since the first report in 2021, the catalytic asymmetric synthesis of N—N atropisomers has developed rapidly into an emerging area. -
封面介绍A Lewis acid-catalyzed [2＋4] cyclization of 3-alkyl- 2-vinylindoles with α,β-unsaturated N?sulfonyl keti- mines is reported by Sun, Sun, Wang, Wu, Wang, Liu, and Zhang on page 2178. This work has confronted the challenges in exploring the [2＋4] cyclization of 3-alkyl-2-vinylindoles, which will enrich the chemistry of 3-alkyl-2-vinylindoles. In addition, this approach provides an atom-economic method for the synthesis of indole-containing piperidines. -
封面介绍The research progress of silver-mediated synthesis of C(3)-disubstituted indolin-2-ones via tandem radical addition/cyclization of N-arylacrylamides is summarized by Ren, Luo, and Zhou on page 2026. These silver- mediated radical alkene difunctionalization transfor- mations are classified according to different types of bond formation.
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本期栏目
目录
综述与进展
有机化学
2023, 43 (6), pp 1899-1933
DOI: 10.6023/cjoc202210017
有机化学
2023, 43 (6), pp 1934-1951
DOI: 10.6023/cjoc202303001
有机化学
2023, 43 (6), pp 1952-1962
DOI: 10.6023/cjoc202210030
有机化学
2023, 43 (6), pp 1963-1976
DOI: 10.6023/cjoc202212024
有机化学
2023, 43 (6), pp 1977-1990
DOI: 10.6023/cjoc202212003
有机化学
2023, 43 (6), pp 1991-2001
DOI: 10.6023/cjoc202211024
有机化学
2023, 43 (6), pp 2002-2025
DOI: 10.6023/cjoc202211006
有机化学
2023, 43 (6), pp 2026-2039
DOI: 10.6023/cjoc202211003
有机化学
2023, 43 (6), pp 2040-2052
DOI: 10.6023/cjoc202210015
有机化学
2023, 43 (6), pp 2053-2067
DOI: 10.6023/cjoc202209005
有机化学
2023, 43 (6), pp 2068-2080
DOI: 10.6023/cjoc202210024
有机化学
2023, 43 (6), pp 2081-2095
DOI: 10.6023/cjoc202210034
研究论文
有机化学
2023, 43 (6), pp 2096-2103
DOI: 10.6023/cjoc202212002
有机化学
2023, 43 (6), pp 2104-2109
DOI: 10.6023/cjoc202212014
有机化学
2023, 43 (6), pp 2110-2119
DOI: 10.6023/cjoc202208010
有机化学
2023, 43 (6), pp 2120-2125
DOI: 10.6023/cjoc202211035
有机化学
2023, 43 (6), pp 2126-2135
DOI: 10.6023/cjoc202209040
有机化学
2023, 43 (6), pp 2136-2142
DOI: 10.6023/cjoc202211004
有机化学
2023, 43 (6), pp 2143-2155
DOI: 10.6023/cjoc202209033
有机化学
2023, 43 (6), pp 2156-2162
DOI: 10.6023/cjoc202210002
有机化学
2023, 43 (6), pp 2163-2170
DOI: 10.6023/cjoc202210029
有机化学
2023, 43 (6), pp 2171-2177
DOI: 10.6023/cjoc202208006
有机化学
2023, 43 (6), pp 2178-2188
DOI: 10.6023/cjoc202210037
有机化学
2023, 43 (6), pp 2189-2196
DOI: 10.6023/cjoc202210020
有机化学
2023, 43 (6), pp 2197-2205
DOI: 10.6023/cjoc202209011
有机化学
2023, 43 (6), pp 2206-2216
DOI: 10.6023/cjoc202208027
有机化学
2023, 43 (6), pp 2217-2225
DOI: 10.6023/cjoc202210027
有机化学
2023, 43 (6), pp 2226-2238
DOI: 10.6023/cjoc202210007
有机化学
2023, 43 (6), pp 2239-2244
DOI: 10.6023/cjoc202209012
研究简报
有机化学
2023, 43 (6), pp 2245-2251
DOI: 10.6023/cjoc202211014
亮点述评
有机化学
2023, 43 (6), pp 2252-2253
DOI: 10.6023/cjoc202300031
有机化学
2023, 43 (6), pp 2254-2255
DOI: 10.6023/cjoc202300032
有机化学
2023, 43 (6), pp 2256-2258
DOI: 10.6023/cjoc202300033
有机化学
2023, 43 (6), pp 2259-2260
DOI: 10.6023/cjoc202300034
有机化学
2023, 43 (6), pp 2261-2263
DOI: 10.6023/cjoc202300035
有机化学
2023, 43 (6), pp 2264-2266
DOI: 10.6023/cjoc202300036
有机化学
2023, 43 (6), pp 2267-2268
DOI: 10.6023/cjoc202300037
