First direct access to 2-hydroxybenzophenones via nickel-catalyzed cross-coupling of 2-hydroxybenzaldehydes with aryl iodides

RSC Advances ◽  
2015 ◽  
Vol 5 (124) ◽  
pp. 102448-102453 ◽  
Author(s):  
N. Nowrouzi ◽  
M. Zarei ◽  
F. Roozbin
Keyword(s):  
Ethylene Glycol ◽  
Cross Coupling ◽  
Direct Access ◽  
Aryl Iodides

The Nickel-catalyzed cross-coupling of 2-hydroxybenzaldehydes with aryl iodides proceeds in ethylene glycol to give the corresponding 2-hydroxybenzophenones.

Nickel-Catalyzed Reductive Cross-Coupling of Benzylic Sulfonium Salts with Aryl Iodides

Synlett ◽  
2022 ◽  
Author(s):  
Fan Wu ◽  
Wei Wang ◽  
Ken Yao
Keyword(s):  
Electron Transfer ◽  
Transfer Process ◽  
Bond Cleavage ◽  
Cross Coupling ◽  
Direct Access ◽  
Single Electron Transfer ◽  
Mechanistic Studies ◽  
Electron Transfer Process ◽  
Sulfonium Salts ◽  
Aryl Iodides

A nickel-catalyzed cross-electrophile coupling of benzylic sulfonium salts with aryl iodides has been developed, providing direct access to diarylalkanes from readily available and stable coupling partners. Preliminary mechanistic studies suggest that the C–S bond cleavage proceeds through a single-electron transfer process to generate a benzylic radical.

Copper-catalyzed carbonylative Suzuki coupling of aryl iodides with arylboronic acids under ambient pressure of carbon monoxide

RSC Advances ◽  
2014 ◽  
Vol 4 (83) ◽  
pp. 44312-44316 ◽  
Author(s):  
Laijin Cheng ◽  
Yanzhen Zhong ◽  
Zhuchao Ni ◽  
Hongyan Du ◽  
Fengli Jin ◽  
...  
Keyword(s):  
Carbon Monoxide ◽  
Ethylene Glycol ◽  
Ambient Pressure ◽  
Cross Coupling ◽  
Suzuki Coupling ◽  
Poly Ethylene Glycol ◽  
Arylboronic Acids ◽  
Aryl Iodides ◽  
Poly Ethylene

An efficient and ligandless nanocopper-catalyzed carbonylative cross-coupling of aryl iodides with arylboronic acids at ambient CO pressure in poly(ethylene glycol), has been developed.

scholarly journals Nickel-Catalyzed Asymmetric Reductive Cross-Coupling of α-Chloroesters with (Hetero)Aryl Iodides

2021 ◽  
Author(s):  
Travis DeLano ◽  
Sara Dibrell ◽  
Caitlin R. Lacker ◽  
Adam Pancoast ◽  
Kelsey Poremba ◽  
...  
Keyword(s):  
Cross Coupling ◽  
Mild Conditions ◽  
Aryl Iodides ◽  
Reaction Proceeds

An asymmetric reductive cross-coupling of α-chloroesters and (hetero)aryl iodides is reported. This nickel-catalyzed reaction proceeds with a chiral BiOX ligand under mild conditions, affording α-arylesters in good yields and enantioselectivities....

Photoinduced Cross-Coupling of Aryl Iodides with Alkenes

2021 ◽  
Author(s):  
Yuliang Liu ◽  
Haoyu Li ◽  
Shunsuke Chiba
Keyword(s):  
Cross Coupling ◽  
Aryl Iodides

scholarly journals Iron/copper-catalyzed C–C cross-coupling of aryl iodides with terminal alkynes

2008 ◽  
Vol 49 (41) ◽  
pp. 5961-5964 ◽  
Author(s):  
Chandra M. Rao Volla ◽  
Pierre Vogel
Keyword(s):  
Cross Coupling ◽  
Terminal Alkynes ◽  
Iron Copper ◽  
Aryl Iodides

An Efficient Copper-Catalyzed Cross-Coupling Reaction of Thiols with Aryl Iodides

2011 ◽  
Vol 2011 (9) ◽  
pp. 1776-1781 ◽  
Author(s):  
Hsin-Lun Kao ◽  
Chin-Keng Chen ◽  
Yu-Jen Wang ◽  
Chin-Fa Lee
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
Aryl Iodides ◽  
Cross Coupling Reaction
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