ChemInform Abstract: A Highly Efficient Pd(PPh3)4-Catalyzed Suzuki Cross-Coupling Method for the Preparation of 2-Nitrobiphenyls from 1-Chloro-2-nitrobenzenes and Phenylboronic Acids.

ChemInform ◽  
2016 ◽  
Vol 47 (29) ◽  
Author(s):  
Vijayaragavan Elumalai ◽  
Alexander H. Sandtorv ◽  
Hans-Rene Bjoersvik
2016 ◽  
Vol 12 ◽  
pp. 2250-2255 ◽  
Author(s):  
Cui Chen ◽  
Weibing Liu ◽  
Peng Zhou

A TBHP-mediated dehydrogenative cross-oxidative-coupling approach has been developed for the synthesis of N-arylbenzamides from methylarenes and acetanilides. This cross-coupling method is free of transition metal catalysts and ligands, and no extra organic solvents are required, which make it an useful and attractive strategy for the straightforward construction of C–N bonds. Besides, this conversion is an important complement to the conventional C–N forming strategies.


2000 ◽  
Vol 65 (11) ◽  
pp. 1683-1697 ◽  
Author(s):  
Michal Hocek ◽  
Antonín Holý ◽  
Ivan Votruba ◽  
Hana Dvořáková

9-(2-Deoxy-β-D-erythro-pentofuranosyl)-6-(4-substituted phenyl)purines, 9-(5-deoxy-β-D-ribofuranosyl)-6-(4-substituted phenyl)purines and 9-(2,3-dihydroxypropyl)-6-(4-substituted phenyl)purines were prepared by the Suzuki-Miyaura cross-coupling reactions of the corresponding protected 9-substituted 6-chloropurines with substituted phenylboronic acids followed by MeONa mediated deprotection. In contrast to the highly active 6-phenylpurine ribonucleosides, the title compounds did not show any considerable cytostatic activity.


ChemInform ◽  
2005 ◽  
Vol 36 (5) ◽  
Author(s):  
Fuk Yee Kwong ◽  
Wai Har Lam ◽  
Chi Hung Yeung ◽  
Kin Shing Chan ◽  
Albert S. C. Chan

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