Experimental and Theoretical Investigations of the Stereoselective Synthesis of P-Stereogenic Phosphine Oxides

2015 ◽  
Vol 21 (25) ◽  
pp. 9057-9061 ◽  
Author(s):  
Laurent Copey ◽  
Ludivine Jean-Gérard ◽  
Eric Framery ◽  
Guillaume Pilet ◽  
Vincent Robert ◽  
...  
ChemInform ◽  
2015 ◽  
Vol 46 (44) ◽  
pp. no-no
Author(s):  
Laurent Copey ◽  
Ludivine Jean-Gerard ◽  
Eric Framery ◽  
Guillaume Pilet ◽  
Vincent Robert ◽  
...  

2015 ◽  
Vol 51 (73) ◽  
pp. 13922-13924 ◽  
Author(s):  
Qingwen Gui ◽  
Liang Hu ◽  
Xiang Chen ◽  
Jidan Liu ◽  
Ze Tan

An efficient and stereoselective synthesis of vinylphosphonates and phosphine oxides was developed starting from styrenes using AgNO3 as the catalyst and K2S2O8 as the oxidant. Various vinyl-phosphonates and phosphine oxides were synthesized in good yields with excellent regioselectivity.


ChemInform ◽  
2015 ◽  
Vol 46 (40) ◽  
pp. no-no
Author(s):  
Mathieu Dutartre ◽  
Jerome Bayardon ◽  
Marie-Joelle Eymin ◽  
Sylvain Juge

2018 ◽  
Vol 42 (2) ◽  
pp. 63-67 ◽  
Author(s):  
Xiu Gu ◽  
Peng Xie ◽  
Jun Jiang ◽  
Yi Wu ◽  
Lisheng Wang

A highly efficient electrophilic addition of 3-diazooxindoles to H-phosphine oxides under metal-free and base-free conditions is established, leading to phosphinic hydrazides. This method has good chemoselectivity and broad substrate diversity, and provides a facile and green approach for N–P bond formation. The stereoselective synthesis represents a unique example of asymmetric electrophilic addition of diazo compounds as N-terminal electrophiles with phosphorus compounds, affording P-stereogenic phosphinic hydrazides with excellent stereoselectivity.


Sign in / Sign up

Export Citation Format

Share Document