-
-
封面介绍Red light-mediated organic synthesis is reviewed by Zhang, Kong, Zhang, and Jiang on page 3804. It covers representative reaction pathways enabled by 600～700 nm red-light excitation, including single-electron transfer, energy transfer, metal-metal bond homolysis, direct excitation of substrates or complexes, and photoenzymatic catalysis. The review discusses catalyst design, reaction mechanisms, and key factors governing reaction efficiency and selectivity, highlighting red light’s unique merits of deep penetration, low phototoxicity, and mild conditions to suppress undesired excitation and side reactions. -
封面介绍A frustrated ion-pair catalyzed deprotection of acetals and ketals was developed by Yang, Li, Zhang, Zou, Chen, and Jia on page 4067. This protocol enabled rapid and efficient conversion of diverse substrates within 20 min, affording a broad range of carbonyl compounds, including aldehydes, ketones, and complex natural products in high yields. -
封面介绍A photoredox/palladium dual-catalyzed fluoroalkylfluo- rosulfonylation of unactivated olefins was reported by Ma, Liu and co?workers on page 4119. Using aryl trifluoromethyl compounds, 1,4-diazabicyclo[2.2.2]oc- tane bis(sulfur dioxide) adduct (DABSO), and N-fluoro- benzenesulfonimide, the radical sulfur dioxide insertion and fluorination strategy enables one?step installation of fluoroalkyl and fluorosulfonyl groups to access diverse aliphatic sulfonyl fluorides, which can be further diver-sified via SuFEx click chemistry. -
封面介绍N-Vinylamides represent a prominent class of synthetic building blocks that serve as versatile substrates for the construction of cyclic frameworks. The recent advances in cyclization reactions involving N-vinylamides are summarized by Shao, Lin, Xiong, He, and Zou on page 3865. The review describes the synthesis of aminocy-clopropanes, oxazolines, oxazoles, pyridines, and other cyclic compounds, with particular emphasis on reaction mechanisms, substrate scope, stereochemical control, and synthetic applications.
-
-
本期栏目
目录
综述与进展
有机化学
2026, 46 (10), pp 3783-3803
DOI: 10.6023/cjoc202606009
有机化学
2026, 46 (10), pp 3804-3837
DOI: 10.6023/cjoc202604030
有机化学
2026, 46 (10), pp 3838-3864
DOI: 10.6023/cjoc202602015
有机化学
2026, 46 (10), pp 3865-3888
DOI: 10.6023/cjoc202604012
有机化学
2026, 46 (10), pp 3889-3903
DOI: 10.6023/cjoc202603033
有机化学
2026, 46 (10), pp 3904-3932
DOI: 10.6023/cjoc202603001
有机化学
2026, 46 (10), pp 3933-3962
DOI: 10.6023/cjoc202601031
研究论文
有机化学
2026, 46 (10), pp 3963-3969
DOI: 10.6023/cjoc202603030
有机化学
2026, 46 (10), pp 3970-3982
DOI: 10.6023/cjoc202603039
有机化学
2026, 46 (10), pp 3983-3988
DOI: 10.6023/cjoc202603027
有机化学
2026, 46 (10), pp 3989-4001
DOI: 10.6023/cjoc202603015
有机化学
2026, 46 (10), pp 4002-4007
DOI: 10.6023/cjoc202605008
有机化学
2026, 46 (10), pp 4008-4015
DOI: 10.6023/cjoc202604035
有机化学
2026, 46 (10), pp 4016-4022
DOI: 10.6023/cjoc202604022
有机化学
2026, 46 (10), pp 4023-4033
DOI: 10.6023/cjoc202604042
有机化学
2026, 46 (10), pp 4034-4049
DOI: 10.6023/cjoc202601044
有机化学
2026, 46 (10), pp 4050-4055
DOI: 10.6023/cjoc202603024
有机化学
2026, 46 (10), pp 4056-4066
DOI: 10.6023/cjoc202603012
有机化学
2026, 46 (10), pp 4067-4076
DOI: 10.6023/cjoc202604046
有机化学
2026, 46 (10), pp 4077-4086
DOI: 10.6023/cjoc202603040
有机化学
2026, 46 (10), pp 4087-4097
DOI: 10.6023/cjoc202602009
有机化学
2026, 46 (10), pp 4098-4107
DOI: 10.6023/cjoc202603016
有机化学
2026, 46 (10), pp 4108-4118
DOI: 10.6023/cjoc202604015
有机化学
2026, 46 (10), pp 4119-4128
DOI: 10.6023/cjoc202604031
有机化学
2026, 46 (10), pp 4129-4040
DOI: 10.6023/cjoc202604017
有机化学
2026, 46 (10), pp 4141-4151
DOI: 10.6023/cjoc202602014
有机化学
2026, 46 (10), pp 4152-4161
DOI: 10.6023/cjoc202510021
有机化学
2026, 46 (10), pp 4162-4171
DOI: 10.6023/cjoc202601020
有机化学
2026, 46 (10), pp 4172-4181
DOI: 10.6023/cjoc202601037
亮点述评
有机化学
2026, 46 (10), pp 4182-4183
DOI: 10.6023/cjoc202600018
有机化学
2026, 46 (10), pp 4184-4186
DOI: 10.6023/cjoc202600019
有机化学
2026, 46 (10), pp 4187-4188
DOI: 10.6023/cjoc202600020
