Highly Selective Hydroiodination of Carbon-Carbon Double or Triple Bonds

被引:3
|
作者
Yamamoto, Yuki [1 ]
Kawaguchi, Shin-ichi [2 ]
Kodama, Shintaro [1 ]
Nomoto, Akihiro [1 ]
Ogawa, Akiya [1 ]
机构
[1] Osaka Prefecture Univ, Grad Sch Engn, Dept Appl Chem, Osaka 5998531, Japan
[2] Saga Univ, Fac Agr, Ctr Educ & Res Agr Innovat, Saga 8470021, Japan
关键词
Hydroiodination; regio- and stereoselective synthesis; alkene and alkyne activations; green synthesis; cross-coupling; iodine reagents; SURFACE-MEDIATED REACTIONS; CROSS-COUPLING REACTIONS; GENERATED IN-SITU; TERMINAL ALKYNES; PHOTOINDUCED IODOPERFLUOROALKYLATION; B(C6F5)(3)-CATALYZED TRANSFER; CATALYZED HYDROALUMINATION; STEREOSELECTIVE-SYNTHESIS; PERFLUOROALKYL IODIDES; UNSATURATED-COMPOUNDS;
D O I
10.2174/1385272824666191227111257
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Iodine is an element that exhibits characteristic features of heavy halogen, and several compounds containing iodine constitute important synthetic intermediates due to synthetically easy manipulation. To utilize iodine units for organic synthesis, a highly regio- and stereoselective introduction of iodine to versatile building blocks is significant, and a lot of research works for the selective introduction of iodine to alkynes or alkenes have been conducted. In this review article, we describe regio- and stereoselective hydroiodination to multiple bonds of building blocks, and its synthetic applications as key intermediates to construct several important compounds in organic chemistry.
引用
收藏
页码:2153 / 2168
页数:16
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