Formation of dimethylphosphinic acid during alkaline cleavage of tetramethyldiphosphine disulfide

Author(s):  
R. A. Malevannaya ◽  
E. N. Tsvetkov ◽  
M. I. Kabachnik
1963 ◽  
Vol 41 (6) ◽  
pp. 1525-1530 ◽  
Author(s):  
H. R. Allcock

The kinetics of alkaline cleavage of o-nitrobenzyltrimethylsilane were examined in aqueous dioxane media. At high water concentrations, increases in solvent polarity retard the cleavage, as required by a mechanism involving charge dispersion in the transition state. At high dioxane concentrations, solvent polarity increases are accompanied by increases in the rate of reaction, a result which may reflect association between the solvent components.


1977 ◽  
Vol 74 (10) ◽  
pp. 4311-4314 ◽  
Author(s):  
A. B. Cohen ◽  
L. D. Gruenke ◽  
J. C. Craig ◽  
D. Geczy

1948 ◽  
Vol 70 (12) ◽  
pp. 4023-4026 ◽  
Author(s):  
Charles R. Hauser ◽  
Frederic W. Swamer ◽  
Betty I. Ringler

ChemInform ◽  
2010 ◽  
Vol 22 (8) ◽  
pp. no-no
Author(s):  
J. P. GUTHRIE ◽  
J. COSSAR
Keyword(s):  

2009 ◽  
Vol 64 (11-12) ◽  
pp. 1617-1624 ◽  
Author(s):  
Matthias Walter ◽  
Gerhard Maas

Betaines 7a, b and 8a, b have been prepared from 3- and 4-piperidinecarboxylic acid and N,N,N',N'-tetraalkyl-chloroformamidinium chlorides via the corresponding methyl esters. These betaines are highly hygroscopic, thermally very stable, and, with the exception of 7b, have rather low melting points. They undergo a surprisingly facile alkaline cleavage of the hexaalkylguanidinium moiety. They react with dichloromethane by a twofold nucleophilic substitution to form methylene dicarboxylates such as 11. TheNMR (1H, 13C) data of betaines 7 and 8 are discussed


2005 ◽  
Vol 75 (11) ◽  
pp. 1717-1719
Author(s):  
T. A. Saakyan ◽  
A. Kh. Gyul'nazaryan ◽  
N. O. Markaryan ◽  
S. T. Kocharyan
Keyword(s):  

Author(s):  
O. A. Raevskii ◽  
R. R. Shagidullin ◽  
I. D. Morozova ◽  
L. E. Petrova ◽  
F. G. Khalitov

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