Petasis reaction of activated quinoline and isoquinoline with various boronic acids

2005 ◽  
Vol 46 (17) ◽  
pp. 3053-3056 ◽  
Author(s):  
Yu Mi Chang ◽  
Seung Hwan Lee ◽  
Mi Hye Nam ◽  
Min Young Cho ◽  
Young Sang Park ◽  
...  
ChemInform ◽  
2005 ◽  
Vol 36 (34) ◽  
Author(s):  
Yu Mi Chang ◽  
Seung Hwan Lee ◽  
Mi Hye Nam ◽  
Min Young Cho ◽  
Young Sang Park ◽  
...  

2011 ◽  
Vol 64 (1) ◽  
pp. 62 ◽  
Author(s):  
Quentin I. Churches ◽  
James K. Johnson ◽  
Nathan L. Fifer ◽  
Craig A. Hutton

The Petasis three-component coupling reaction of N-benzylphenylglycinol, glyoxylic acid, and styrenylboronic acids allows for the efficient synthesis of functionalized homoarylalanine derivatives. The reactions were shown to proceed in high yield but low selectivity, regardless of the nature of the substituent on the styrenylboronic acid component. Anomalies in the stereoselectivity of these reactions compared with previously reported results have been traced to the source of the organoboronic acid. Asymmetric dihydroxylation of the unsaturated amino acid derivatives enables a highly efficient route to dihydroxyhomoarylalanine derivatives.


Author(s):  
K. Natarajan ◽  
Irfana Jesin C. P. ◽  
A.Antony Haritha Mercy ◽  
Ganesh Chandra Nandi

Herein, we disclose a metal-free novel approach for the synthesis of N-( -substituted)alkyl sulfoximines/sulfonimidamides via one-pot multicomponent Petasis reactions of aryl boronic acids, ortho-hydroxyarylaldehydes and sulfoximines/sulfonimidamides in moderate to very...


iScience ◽  
2021 ◽  
pp. 103134
Author(s):  
Monica Oliva ◽  
Prabhat Ranjan ◽  
Serena Pillitteri ◽  
Guglielmo Attilio Coppola ◽  
Monica Messina ◽  
...  

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,...


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