scholarly journals The modern interpretation of the Wittig reaction mechanism

2013 ◽  
Vol 42 (16) ◽  
pp. 6670 ◽  
Author(s):  
Peter A. Byrne ◽  
Declan G. Gilheany

ChemInform ◽  
2013 ◽  
Vol 44 (41) ◽  
pp. no-no
Author(s):  
Peter A. Byrne ◽  
Declan G. Gilheany


1997 ◽  
Vol 75 (10) ◽  
pp. 1322-1330 ◽  
Author(s):  
Margaret M. Kayser ◽  
Jun Zhu ◽  
Donald L. Hooper

The synthesis of halo enol lactones from cyclic anhydrides via lactonization of the corresponding keto phosphoranes provides a direct route to these interesting compounds, which possess important biological properties and are useful intermediates in organic synthesis. In this paper we outline the syntheses of several halo enol lactones and discuss mechanistic consequences of these reactions on the understanding of Wittig reactions with cyclic anhydrides. Keywords: halolactonization, cyclic anhydrides, halo enol lactones, Wittig reaction mechanism.





Author(s):  
Tomasz J. Idzik ◽  
Zofia M. Myk ◽  
Łukasz Struk ◽  
Magdalena Perużyńska ◽  
Gabriela Maciejewska ◽  
...  

Triisopropylsilyltrifluoromethanesulfonate can be effectively used for the arylation of a wide range of enelactams. The multinuclear NMR study provided deep insights into the reaction mechanism.



2009 ◽  
Author(s):  
Mendel Fleisher ◽  
E. Lukevics ◽  
L. Leite ◽  
D. Jansone ◽  
K. Edolfa ◽  
...  


Clean Air ◽  
2007 ◽  
Vol 8 (1) ◽  
pp. 1-24
Author(s):  
M. Pourkashanian ◽  
N. S. Mera ◽  
Lionel Elliott ◽  
C. W. Wilson ◽  
Derek B. Ingham ◽  
...  


2020 ◽  
Author(s):  
Kiron Kumar Ghosh ◽  
Alexander Uttry ◽  
Francesca Ghiringhelli ◽  
Arup Mondal ◽  
Manuel van Gemmeren

We report the ligand enabled C(sp3)–H activation/olefination of free carboxylic acids in the γ-position. Through an intramolecular Michael-addition, δ-lactones are obtained as products. Two distinct ligand classes are identified that enable the challenging palladium-catalyzed activation of free carboxylic acids in the γ-position. The developed protocol features a wide range of acid substrates and olefin reaction partners and is shown to be applicable on a preparatively useful scale. Insights into the underlying reaction mechanism obtained through kinetic studies are reported.<br>



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