scholarly journals Catalytic cross-coupling of diazo compounds with coinage metal-based catalysts: an experimental and theoretical study

2013 ◽  
Vol 42 (12) ◽  
pp. 4132 ◽  
Author(s):  
Ivan Rivilla ◽  
W. M. C. Sameera ◽  
Eleuterio Alvarez ◽  
M. Mar Díaz-Requejo ◽  
Feliu Maseras ◽  
...  
2015 ◽  
Vol 137 (45) ◽  
pp. 14496-14501 ◽  
Author(s):  
Mingyou Hu ◽  
Chuanfa Ni ◽  
Lingchun Li ◽  
Yongxin Han ◽  
Jinbo Hu

ACS Catalysis ◽  
2020 ◽  
Vol 10 (21) ◽  
pp. 12881-12887
Author(s):  
Zhaohong Liu ◽  
Shanshan Cao ◽  
Jiayi Wu ◽  
Giuseppe Zanoni ◽  
Paramasivam Sivaguru ◽  
...  

2016 ◽  
Vol 45 (9) ◽  
pp. 3706-3710 ◽  
Author(s):  
Xuefei Zhao ◽  
Lionel Perrin ◽  
David J. Procter ◽  
Laurent Maron

The first detailed theoretical study on the synthetically important electron transfer reductant SmI2–H2O has been conducted in the context of the activation of important alkyliodide, ketone, lactone and ester substrates, processes of importance in cross-coupling.


2011 ◽  
Vol 123 (11) ◽  
pp. 2592-2596 ◽  
Author(s):  
Jørn H. Hansen ◽  
Brendan T. Parr ◽  
Philip Pelphrey ◽  
Quihui Jin ◽  
Jochen Autschbach ◽  
...  

2011 ◽  
Vol 50 (11) ◽  
pp. 2544-2548 ◽  
Author(s):  
Jørn H. Hansen ◽  
Brendan T. Parr ◽  
Philip Pelphrey ◽  
Quihui Jin ◽  
Jochen Autschbach ◽  
...  

Author(s):  
Ge Zhang ◽  
Ze-Jian Xue ◽  
Fang Zhang ◽  
Shu-Sheng Zhang ◽  
Meng-Yao Li ◽  
...  

A highly efficient palladium-catalyzed cross-coupling of 2,2-diarylvinyl bromides with diazo compounds was developed, providing a convenient approach for the synthesis of tetrasubsti-tuted allenes. Both aryl diazo carbonyl compounds and N-tosylhydrazones are competent carbene precursors in this reaction. An unprecedented hydrogen elimination of the π-allyl palladium intermediate is proposed to be the key step.


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