Nucleic acids components and their analogues. LVI. 5-Azauracil and its N-methyl derivatives, formation and decomposition in aqueous solutions, structure of compounds with alcohols

1965 ◽  
Vol 30 (1) ◽  
pp. 90-98 ◽  
Author(s):  
P. Piťhová ◽  
A. Pískala ◽  
J. Piťha ◽  
F. Šorm
Nature ◽  
1972 ◽  
Vol 235 (5338) ◽  
pp. 386-388 ◽  
Author(s):  
M. SHIE ◽  
I. G. KHARITONENKOV ◽  
T. I. TIKHONENKO ◽  
Yu. N. CHIRGADZE

1966 ◽  
Vol 19 (5) ◽  
pp. 841 ◽  
Author(s):  
RK Norris ◽  
S Sternhell

On the basis of N.M.R. spectra, supported by u.v. and i.r. data, it can be concluded that "p-nitrosophenol" and several of its methyl derivatives exist predominantly in the benzoquinone monoxime form in organic solvents and that in aqueous solutions the corresponding potassium salts have the negative charge largely on the oxime oxygen. The protons on the α-carbon syn to the quinone monoxime hydroxyl are deshielded with respect to the anti protons but this relationship appears to be reversed in the anions. The N.M.R. spectra of some p-nitrosoanisoles and quinone monoxime methyl ethers are given and syn-anti equilibria and long-range spin-spin coupling are discussed.


2011 ◽  
Vol 13 (13) ◽  
pp. 6260 ◽  
Author(s):  
Wojciech Marczak ◽  
Bożena Czech ◽  
László Almásy ◽  
Didier Lairez

Polymer ◽  
2010 ◽  
Vol 51 (9) ◽  
pp. 1972-1982 ◽  
Author(s):  
Daniela Risica ◽  
Andrea Barbetta ◽  
Luca Vischetti ◽  
Cesare Cametti ◽  
Mariella Dentini

1975 ◽  
Vol 64 (3) ◽  
pp. 581 ◽  
Author(s):  
Salvatore Cannistraro ◽  
Yves Lion ◽  
Albert van de Vorst

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