scholarly journals Synthesis of substituted benzooxaborinin-1-ols via palladium-catalysed cyclisation of alkenyl- and alkynyl-boronic acids

2016 ◽  
Vol 14 (34) ◽  
pp. 8039-8043 ◽  
Author(s):  
Laure Benhamou ◽  
Daniel W. Walker ◽  
Dejan-Krešimir Bučar ◽  
Abil E. Aliev ◽  
Tom D. Sheppard

Substituted benzooxaborinin-1-ols can be preparedviapalladium-catalysed oxidative cyclisation of boronic acids bearing a pendent alkene or alkyne group.

2020 ◽  
Vol 7 (23) ◽  
pp. 3862-3867
Author(s):  
Hua Huang ◽  
Qing-Zhu Li ◽  
Yan-Qing Liu ◽  
Hai-Jun Leng ◽  
Peng Xiang ◽  
...  

A novel intermolecular dearomative [4 + 2] annulation of 3-nitroindoles and enals under oxidative N-heterocyclic carbene catalysis has been developed. This protocol was also suitable for the oxidative cyclisation of 2-nitrobenzothiophenes with enals.


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):  

ACS Catalysis ◽  
2021 ◽  
Vol 11 (17) ◽  
pp. 10862-10870 ◽  
Author(s):  
Prabhat Ranjan ◽  
Serena Pillitteri ◽  
Guglielmo Coppola ◽  
Monica Oliva ◽  
Erik V. Van der Eycken ◽  
...  
Keyword(s):  

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