Palladium-Catalyzed Ring-Opening of 2-Alkylidenecyclobutanols: Stereoselective Synthesis of γ,δ-Unsaturated Ketones by C−C Bond Cleavage

2017 ◽  
Vol 360 (3) ◽  
pp. 411-415 ◽  
Author(s):  
Ling Chen ◽  
Feng-Na Sun ◽  
Yu-Li Sun ◽  
Zheng Xu ◽  
Zhan-Jiang Zheng ◽  
...  
2018 ◽  
Vol 5 (10) ◽  
pp. 1651-1654 ◽  
Author(s):  
Lidong Shan ◽  
Ge Wu ◽  
Miaochang Liu ◽  
Wenxia Gao ◽  
Jinchang Ding ◽  
...  

Palladium-catalyzed ring-opening acylation of cyclopropenones with organoboronic acids (aryl and vinylboronic acids) at room temperature has been developed to synthesise α,β-diaryl unsaturated ketones with good yields and excellent stereospecificity.


Synlett ◽  
2017 ◽  
Vol 29 (06) ◽  
pp. 754-758 ◽  
Author(s):  
Takanori Matsuda ◽  
Takeshi Matsumoto ◽  
Akira Murakami

A palladium(0)-catalyzed ring-opening cross-coupling reaction between tert-cyclobutenols and aryl halides produces γ-arylated β,γ-unsaturated ketones. In the case of aryl halides bearing functional groups at the ortho position, the resulting ring-opened ketones undergo intramolecular condensation to afford bicyclic aromatic compounds.


2020 ◽  
Vol 7 (18) ◽  
pp. 2731-2736 ◽  
Author(s):  
Xin-Xing Wu ◽  
Hao Ye ◽  
Hong Dai ◽  
Bing Yang ◽  
Yang Wang ◽  
...  

An efficient cascade dienylation provides a range of alkylated conjugated diene compounds with the Z-configuration by introducing the C4 unit directly.


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