Palladium-Catalyzed Cross-Coupling Reactions of 4-Tosyl-2(5H)-furanone with Boronic Acids:  A Facile and Efficient Route to Generate 4-Substituted 2(5H)-Furanones

2003 ◽  
Vol 68 (2) ◽  
pp. 670-673 ◽  
Author(s):  
Jie Wu ◽  
Qiang Zhu ◽  
Lisha Wang ◽  
Reza Fathi ◽  
Zhen Yang
Synlett ◽  
2009 ◽  
Vol 2010 (02) ◽  
pp. 211-214
Author(s):  
Man-Kin Tse ◽  
Naveenkumar Mangu ◽  
Anke Spannenberg ◽  
Matthias Beller

2016 ◽  
Vol 69 (6) ◽  
pp. 618 ◽  
Author(s):  
Bhaskaran Savitha ◽  
Ayyiliath. M. Sajith ◽  
M. Nibin Joy ◽  
K.K. Abdul Khader ◽  
A. Muralidharan ◽  
...  

In this paper, we report the use of potassium organotrifluoroborate salts as nucleophilic organoboron reagents in the Suzuki cross-coupling reactions of 2-halo deazapurines. Regio-isomeric C-2-substituted imidazo[4,5-b]pyridine analogues were synthesized by employing this protocol in good to excellent yields. Whereas aryl and heteroaryl trifluoroborates reacted readily to give the coupled products in high yields, alkyltrifluoroborates were found to be less reactive. The utilization of tetrabutylammonium acetate was found to play a substantial role in enhancing the reaction rates of the cross-coupling process. Also, a comparative study was performed between boronic acids and potassium organotrifluoroborate salts.


2009 ◽  
Vol 21 ◽  
pp. S124-S126 ◽  
Author(s):  
Shaoyan WANG ◽  
Zhiqiang ZHANG ◽  
Zhizhi HU ◽  
Yue WANG ◽  
Peng LEI ◽  
...  

2021 ◽  
Author(s):  
Hari Balakrishnan Madasamy ◽  
Kanagaraj Madasamy ◽  
Velayutham Sankar ◽  
Mahesh kumar Ravva ◽  
Mannathan Subramaniyan

An efficient palladium-catalyzed denitrogenative Suzuki-Miyaura type cross-coupling of 1,2,3-benzotriazin-4(3H) ones with organoboronic acid is described. The reaction is compatible with various aryl and alkenyl boronic acids affording ortho-arylated and alkenylated...


2015 ◽  
Vol 145 (8) ◽  
pp. 1634-1642 ◽  
Author(s):  
Chengcai Xia ◽  
Yong Yang ◽  
Zhenjiang Wei ◽  
Wenbo Yu ◽  
Hanxiao Liao ◽  
...  

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