Synthesis of Flufenamic Acid: An Organic Chemistry Lab Sequence Using Boronic Acids and Nitrosoarenes under Transition-Metal-Free Conditions

2019 ◽  
Vol 96 (8) ◽  
pp. 1738-1744 ◽  
Author(s):  
Silvia Roscales ◽  
Aurelio G. Csákÿ

2020 ◽  
Vol 61 (43) ◽  
pp. 152444
Author(s):  
Hao Ding ◽  
Wan-Ying Qi ◽  
Jing-Song Zhen ◽  
Qiuping Ding ◽  
Yong Luo




2016 ◽  
Vol 52 (14) ◽  
pp. 3018-3021 ◽  
Author(s):  
S. Roscales ◽  
A. G. Csákÿ

We describe the first ring-opening of furfuryl alcohols with boronic acids to afford functionalized γ-ketoaldehydes.



Synthesis ◽  
2016 ◽  
Vol 48 (14) ◽  
pp. 2165-2177 ◽  
Author(s):  
Aurelio Csákÿ ◽  
Francisco Sánchez-Sancho


2020 ◽  
Author(s):  
Lucía Florentino ◽  
Lucía López ◽  
Raquel Barroso ◽  
María‐Paz Cabal ◽  
Carlos Valdés


2020 ◽  
Vol 26 (46) ◽  
pp. 10591-10597
Author(s):  
Keith Livingstone ◽  
Sophie Bertrand ◽  
Alan R. Kennedy ◽  
Craig Jamieson


2020 ◽  
Vol 2020 ◽  
pp. 1-7 ◽  
Author(s):  
Tanveer MahmadAlli Shaikh

An alternate procedure for oxidative hydroxylation of aryl boronic acids with aqueous TBHP to access phenols is described. The protocol tolerated various functional groups substituted with aromatic rings. The reaction was performed in water and free from transition metal oxidants.





2013 ◽  
Vol 52 (22) ◽  
pp. 5684-5686 ◽  
Author(s):  
Vincent Coeffard ◽  
Xavier Moreau ◽  
Christine Thomassigny ◽  
Christine Greck


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