Schiff Base/CuI as a Novel Efficient Catalyst System for Cu–Catalyzed Heck Reaction in Water

2019 ◽  
Vol 4 (33) ◽  
pp. 9673-9676
Author(s):  
Yufang Wang ◽  
Mingjie Zhang
Synlett ◽  
2018 ◽  
Vol 29 (16) ◽  
pp. 2081-2086 ◽  
Author(s):  
Stephen Newman ◽  
Jaya Vandavasi

The classical Heck reaction is among the most powerful methods available for the construction of C–C bonds. Modification of this transformation to utilize diverse organohalide coupling partners has resulted in new reactions such as the silyl-Heck, aza-Heck, and boryl-Heck reactions. In contrast, modification of the olefin coupling partner is rare. For instance, use of the π-bond of an aldehyde instead of an alkene would provide ketones via a carbonyl-Heck process. This seemingly minor manipulation of the Heck reaction has proven surprisingly difficult to realize in practice. Through the use of high-throughput ­experimentation techniques, an efficient catalyst system for this transformation was identified, enabling the intermolecular coupling of ­organotriflates and aldehydes to synthesize diverse ketones.


2012 ◽  
Vol 23 (6) ◽  
pp. 690-694 ◽  
Author(s):  
Guang Peng Zhou ◽  
Yong Hai Hui ◽  
Ning Ning Wan ◽  
Qiu Ju Liu ◽  
Zheng Feng Xie ◽  
...  

ChemInform ◽  
2013 ◽  
Vol 44 (3) ◽  
pp. no-no
Author(s):  
Guang Peng Zhou ◽  
yong Hai Hui ◽  
Ning Ning Wan ◽  
Qiu Ju Liu ◽  
Zheng Feng Xie ◽  
...  

2019 ◽  
Vol 149 (8) ◽  
pp. 2142-2157 ◽  
Author(s):  
Samim Sultana ◽  
Geetika Borah ◽  
Pradip. K. Gogoi

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