Synthesis of Tetrasubstituted Furans by Using Photoredox‐Catalyzed Coupling of 2‐Bromo‐1,3‐dicarbonyl Compounds with Silyl Enol Ethers

2016 ◽  
Vol 6 (4) ◽  
pp. 414-417 ◽  
Author(s):  
Yue‐Yue Han ◽  
Yan‐Yan Jiao ◽  
Daan Ren ◽  
Zhentao Hu ◽  
Sheng Shen ◽  
...  
1997 ◽  
Vol 75 (7) ◽  
pp. 965-974 ◽  
Author(s):  
M. Anne Charlton ◽  
James R. Green

Ester-substituted allyltetracarbonyliron cations react with cycloalkylidene-type silyl enol ethers, silyl ketene acetals, and β-keto-esters to give 1,6-dicarbonyl compounds containing a newly formed quaternary centre. Selected condensation products are converted by enolate chemistry into spirocyclic [4.4], [4.5], and [4.6] systems. Acyloin and other reductive cyclization reactions are employed to convert the condensation products into spirocyclic [4.5], [5.5], and [5.6] systems. Keywords: allyliron complexes, umpolung synthesis, 1,6-dicarbonyls, spirocycle synthesis.


2014 ◽  
Vol 18 (5) ◽  
pp. 525-546 ◽  
Author(s):  
Carmen Hernandez-Cervantes ◽  
Miriam Alvarez-Corral ◽  
Manuel Munoz-Dorado ◽  
Ignacio Rodriguez-Garcia

Author(s):  
Kohsuke Aikawa ◽  
KyoKo Nozaki ◽  
Takashi Okazoe ◽  
Yuichiro Ishibashi ◽  
Akiya Adachi

ChemInform ◽  
2010 ◽  
Vol 23 (48) ◽  
pp. no-no
Author(s):  
E. C. ROOS ◽  
H. HIEMSTRA ◽  
W. N. SPECKAMP ◽  
B. KAPTEIN ◽  
J. KAMPHUIS ◽  
...  

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