Recent Progress in N-Iodosuccinimide (NIS)-Mediated Iodination Reactions

被引:3
作者
Cao Tongyang [1 ]
Li Wei [1 ,2 ]
Wang Lijing [1 ,2 ]
机构
[1] Hebei Univ, Coll Chem & Mat Sci, Baoding 071002, Hebei, Peoples R China
[2] Minist Educ, Key Lab Chem Biol Hebei Prov, Key Lab Med Chem & Mol Diag, Baoding 071002, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
iodization; N-iodosuccinimide; organoiodine compounds; TERMINAL ALKYNES; EFFICIENT SYNTHESIS; MEDIATED REACTION; ACCESS; CYCLIZATION; ACIDS; IODOETHERIFICATION; FUNCTIONALIZATION; HALOAZIDATION; 1-HALOALKYNES;
D O I
10.6023/cjoc202306026
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Organoiodine compounds belong to a very important class of functional molecules and their synthesis research is of great significance. Given the advantages of N-iodosuccinimide (NIS) with high reactivity, cheap and easy to get and environmental friendliness, it has always been the preferred iodine reagent for iodization, and in recent years, the preparation of organic iodine compounds by iodization reaction with NIS has made great progress, which has received considerable interest. To this end, the research progress is summarized, including the C-H iodization of NIS and aromatics/terminal alkynes, iodine difunctionalization between NIS and unsaturated compounds with nucleophiles, and cascade iodocyclization between NIS and unsaturated compounds.
引用
收藏
页码:508 / 524
页数:17
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