Synthesis of substituted cinnamic acids by the Heck reaction in aqueous media

Author(s):  
N. A. Bumagin ◽  
N. P. Andryukhova ◽  
I. P. Beletskaya
2008 ◽  
Vol 41 (4) ◽  
pp. 429-432 ◽  
Author(s):  
Petra Moravčíková ◽  
Peter Fodran ◽  
Emil Kolek ◽  
Vlasta Brezová

2015 ◽  
Vol 39 (10) ◽  
pp. 7988-7997 ◽  
Author(s):  
Barahman Movassagh ◽  
Nasrin Rezaei

We have prepared a highly active and recyclable heterogeneous catalyst for the Heck reaction in aqueous media in high yields.


Synlett ◽  
2006 ◽  
Vol 2006 (18) ◽  
pp. 2959-2964 ◽  
Author(s):  
Carmen Nájera ◽  
Emilio Alacid
Keyword(s):  

2018 ◽  
Vol 16 (42) ◽  
pp. 7971-7983 ◽  
Author(s):  
Gopinathan Muthusamy ◽  
Sunil V. Pansare

Stereoselective hydroacyloxylation of iodoalkynes with β-aryl cinnamic acids and subsequent Mizoroki–Heck reaction provides an efficient route to substituted 2(3H)-furanones.


Tetrahedron ◽  
2011 ◽  
Vol 67 (1) ◽  
pp. 250-256 ◽  
Author(s):  
Shang Wu ◽  
Hengchang Ma ◽  
Xiaojie Jia ◽  
Yunmei Zhong ◽  
Ziqiang Lei

2008 ◽  
Vol 49 (27) ◽  
pp. 4252-4255 ◽  
Author(s):  
Shivaji S. Pawar ◽  
Deepak V. Dekhane ◽  
Murlidhar S. Shingare ◽  
Shivaji N. Thore

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