A FACILE PREPARATION OF 3-HALOFLAVONES USING HYPERVALENT IODINE* CHEMISTRY

2001 ◽  
Vol 31 (14) ◽  
pp. 2101-2106 ◽  
Author(s):  
Ho Sik Rho ◽  
Byoung-Seob Ko ◽  
Young-Sung Ju
ChemInform ◽  
2010 ◽  
Vol 32 (45) ◽  
pp. no-no
Author(s):  
Ho Sik Rho ◽  
Byoung-Seob Ko ◽  
Young-Sung Ju

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Xuemin Li ◽  
Guangchen Li ◽  
Yifu Cheng ◽  
Yunfei Du

Abstract The application of hypervalent iodine species generated in situ in organic transformations has emerged as a useful and powerful tool in organic synthesis, allowing for the construction of a series of bond formats via oxidative coupling. Among these transformations, the catalytic aryl iodide can be oxidized to hypervalent iodine species, which then undergoes oxidative reaction with the substrates and the aryl iodine regenerated again once the first cyclic cycle of the reaction is completed. This review aims to systematically summarize and discuss the main progress in the application of in situ-generated hypervalent iodine species, providing references and highlights for synthetic chemists who might be interested in this field of hypervalent iodine chemistry.


Daxue Huaxue ◽  
2019 ◽  
Vol 34 (2) ◽  
pp. 1-16
Author(s):  
Dan LIU ◽  
◽  
Jiahao HE ◽  
Chi ZHANG

Tetrahedron ◽  
2010 ◽  
Vol 66 (31) ◽  
pp. 5737-5738 ◽  
Author(s):  
Stéphane Quideau ◽  
Thomas Wirth

2019 ◽  
Vol 17 (34) ◽  
pp. 7822-7848 ◽  
Author(s):  
I. F. Dempsey Hyatt ◽  
Loma Dave ◽  
Navindra David ◽  
Kirandeep Kaur ◽  
Marly Medard ◽  
...  

This review covers recent developments of hypervalent iodine chemistry in dearomatizations, radicals, hypervalent iodine-guided electrophilic substitution, arylations, photoredox, and more.


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