Ruthenium(II)-Catalyzed CH Arylation of Anilides with Boronic Acids, Borinic Acids and Potassium Trifluoroborates

2015 ◽  
Vol 357 (2-3) ◽  
pp. 474-480 ◽  
Author(s):  
Jonathan Hubrich ◽  
Thomas Himmler ◽  
Lars Rodefeld ◽  
Lutz Ackermann
2015 ◽  
Vol 21 (36) ◽  
pp. 12667-12675 ◽  
Author(s):  
Bram Verbelen ◽  
Lucas Cunha Dias Rezende ◽  
Stijn Boodts ◽  
Jeroen Jacobs ◽  
Luc Van Meervelt ◽  
...  

ChemInform ◽  
2015 ◽  
Vol 46 (26) ◽  
pp. no-no
Author(s):  
Jonathan Hubrich ◽  
Thomas Himmler ◽  
Lars Rodefeld ◽  
Lutz Ackermann

2020 ◽  
Author(s):  
Aidan Kelly ◽  
Peng-Jui (Ruby) Chen ◽  
Jenna Klubnick ◽  
Daniel J. Blair ◽  
Martin D. Burke

<div> <div> <div> <p>Existing methods for making MIDA boronates require harsh conditions and complex procedures to achieve dehydration. Here we disclose that a pre-dried form of MIDA, MIDA anhydride, acts as both a source of the MIDA ligand and an in situ desiccant to enable a mild and simple MIDA boronate synthesis procedure. This method expands the range of sensitive boronic acids that can be converted into their MIDA boronate counterparts. Further utilizing unique properties of MIDA boronates, we have developed a MIDA Boronate Maker Kit which enables the direct preparation and purification of MIDA boronates from boronic acids using only heating and centrifuge equipment that is widely available in labs that do not specialize in organic synthesis. </p> </div> </div> </div>


2014 ◽  
Vol 21 (10) ◽  
pp. 1004-1010
Author(s):  
Guohua Chen ◽  
Xiangying Gu ◽  
Lin Chen ◽  
Xin Wang ◽  
Yue-Lei Chen ◽  
...  
Keyword(s):  

Author(s):  
Pan Xie ◽  
Cheng Xue ◽  
Cancan Wang ◽  
Dongdong Du ◽  
Sanshan Shi

A CF3SO2Na/Pd(OAc)2 co-catalyzed strategy is developed to produce aryl ketones via visible-light-induced decarboxylative cross-coupling of α-oxocarboxylic acids and aryl boronic acids. This process was perfomed under air at room temperature,...


Synthesis ◽  
2021 ◽  
Author(s):  
Hengyuan Li ◽  
Chuanle Zhu

The three-starting materials four-component reaction of (trifluoromethyl)alkenes, TBHP, and boronic acids is reported, delivering various useful α-trifluoromethyl-β-aryloxy tertiary alcohols in high yields and in an exclusively regioselective hydroetherification manner. TBHP serves as both the oxidants and the nucleophiles in this reaction, as well as the O-source of the products.


2021 ◽  
Vol 68 ◽  
pp. 152897
Author(s):  
Kui Lu ◽  
Xiaolan Xi ◽  
Ting Zhou ◽  
Lingyu Lei ◽  
Quan Li ◽  
...  
Keyword(s):  

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