New method for synthesis of bifunctional tertiary phosphine oxides

Author(s):  
V. K. Khairullin ◽  
G. V. Dmitrieva ◽  
I. A. Aleksandrova ◽  
M. A. Vasyanina
2016 ◽  
Vol 81 (17) ◽  
pp. 7644-7653 ◽  
Author(s):  
Ji-Ping Wang ◽  
Shao-Zhen Nie ◽  
Zhong-Yang Zhou ◽  
Jing-Jing Ye ◽  
Jing-Hong Wen ◽  
...  

1997 ◽  
Vol 127 (1) ◽  
pp. 27-37 ◽  
Author(s):  
S. V. Arbanov ◽  
T. Toshev A ◽  
E. Russev A

1980 ◽  
Vol 11 (32) ◽  
Author(s):  
U. M. DZHEMILEV ◽  
L. YU. GUBAIDULLIN ◽  
G. A. TOLSTIKOV ◽  
L. M. ZELENOVA
Keyword(s):  

1985 ◽  
Vol 26 (6) ◽  
pp. 783-786 ◽  
Author(s):  
Tsuneo Imamoto ◽  
Kazuhiko Sato ◽  
Carl R. Johnson

1985 ◽  
Vol 16 (48) ◽  
Author(s):  
S. VARBANOV ◽  
V. VASILEVA ◽  
V. ZLATEVA ◽  
T. RADEVA ◽  
G. BORISOV

1975 ◽  
Vol 53 (10) ◽  
pp. 1468-1474 ◽  
Author(s):  
Edmund Malinski ◽  
Antonina Piekos ◽  
Tomasz A. Modro

The nitration of some tertiary phosphine oxides ArP(O)R2 in aqueous sulfuric acid has been investigated. All compounds studied react as conjugate acids. When the phosphinyl group is bonded directly to the benzene ring, high deactivation and meta-orientation is found, accompanied in most cases by some substitution at the ortho position. The substituent effects of the "quasiphosphonium" group P(OH)R2+are compared with those of structurally related systems and are discussed in terms of pπ–dπ, interactions of the oxygen and the phosphorus atom.


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