Reaction of dialkyl phosphonates with hexafluoroacetone

1970 ◽  
Vol 48 (13) ◽  
pp. 1987-1990 ◽  
Author(s):  
A. F. Janzen ◽  
R. Pollitt

The reaction of dialkyl phosphonates, (RO)2P(O)H where R = CH3, C2H5, and n-C4H9, with hexafluoroacetone gives, in each case, two isomeric products, (RO)2P(O)OCH(CF3)2 and (RO)2P(O)C(OH)-(CF3)2. Products are characterized by elemental analyses, infrared, proton and fluorine nuclear magnetic resonance, and mass spectrometry. The relative yield of isomer depends markedly on the alkyl group present. These results are explained in terms of an inductive effect on the polarity of the P—H bond which influences the direction of addition of hexafluoroacetone.

2020 ◽  
Vol 56 (62) ◽  
pp. 8814-8817 ◽  
Author(s):  
Monika Kijewska ◽  
Angelika Czerwińska ◽  
Samah Al-Harthi ◽  
Grzegorz Wołczański ◽  
Mateusz Waliczek ◽  
...  

The intramolecular interactions between the fructosyl moiety and phenylboronic acid incorporated into various positions of the peptide chain were investigated using mass spectrometry (MS), circular dichroism (CD), and nuclear magnetic resonance (NMR).


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