Mild and Ligand-Free Palladium-Catalyzed Cross-Couplings Between Aryl Halides and Arylboronic Acids for the Synthesis of Biaryls and Heterocycle-Containing Biaryls.

ChemInform ◽  
2007 ◽  
Vol 38 (28) ◽  
Author(s):  
Chen-Liang Deng ◽  
Sheng-Mei Guo ◽  
Ye-Xiang Xie ◽  
Jin-Heng Li
ChemInform ◽  
2014 ◽  
Vol 45 (16) ◽  
pp. no-no
Author(s):  
Luca Basolo ◽  
Alice Bernasconi ◽  
Gianluigi Broggini ◽  
Silvia Gazzola ◽  
Egle M. Beccalli

RSC Advances ◽  
2014 ◽  
Vol 4 (99) ◽  
pp. 55732-55737 ◽  
Author(s):  
Nasser Iranpoor ◽  
Habib Firouzabadi ◽  
Khashayar Rajabi Moghadam ◽  
Somayeh Motavalli

ChemInform ◽  
2010 ◽  
Vol 41 (44) ◽  
pp. no-no
Author(s):  
Eunjin Song ◽  
Jinhyung Park ◽  
Il-Kwon Oh ◽  
Hyun Min Jung ◽  
Sunwoo Lee

ChemInform ◽  
2005 ◽  
Vol 36 (28) ◽  
Author(s):  
Steven A. Weissman ◽  
Daniel Zewge ◽  
Cheng Chen

Synlett ◽  
2021 ◽  
Author(s):  
Zhiyuan Yang ◽  
Pei-Xue Gong ◽  
Junjie Chen ◽  
Jie Zhang ◽  
Xu Gong ◽  
...  

A ligand-free palladium-catalyzed carbonylation of vinyl iodides with arylboronic acids allowing for the synthesis of chalcones and α-branched enones has been established. This reaction proceeds smoothly under ambient pressure and temperature and even use of substoichiometric base renders the transformation to work well. Importantly, this mild, efficient, operationally simple protocol is suitable for the late-stage functionalization of an epiandrosterone-derived complex molecule.


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