scholarly journals Hypervalent Iodine Chemistry and Light: Photochemical Reactions Involving Hypervalent Iodine Chemistry

ARKIVOC ◽  
2021 ◽  
Vol 2021 (7) ◽  
Author(s):  
Fateh V Singh ◽  
Thomas Wirth
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.


2001 ◽  
Vol 31 (14) ◽  
pp. 2101-2106 ◽  
Author(s):  
Ho Sik Rho ◽  
Byoung-Seob Ko ◽  
Young-Sung Ju

SynOpen ◽  
2021 ◽  
Author(s):  
Addison M Duda ◽  
Michael T Giurini ◽  
Jason G Gillmore ◽  
Thomas F Guarr

Synthetic preparation of carbazoles can be challenging, requiring ring building strategies and/or precious metal catalysts. Presented herein is a method for preparation of carbazoles with the use of inexpensive and reliable hypervalent iodine chemistry. An oxidative single electron transfer (SET) event initiates cyclization for preparation of our trifluoromethyl carbazoles. This method has been shown to be useful for a variety of bis(trifluoromethyl)carbazole isomers that are of primary interest for use as battery materials.


2022 ◽  
pp. 335-386
Author(s):  
Brandon Frey † ◽  
Asim Maity † ◽  
Hao Tan ◽  
Pritam Roychowdhury ◽  
David C. Powers

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