88708-60-5Relevant academic research and scientific papers
FLUORIDE ION INDUCED TERMINAL OLEFIN SYNTHESIS FROM β-HYDROXYALKYLPHOSPHONATES
Kawashima, Takayuki,Ishii, Takafumi,Inamoto, Naoki
, p. 1375 - 1378 (1983)
β-Hydroxyalkylphosphonates, prepared readily from alkylphosphonates and carbonyl compounds, were treated with a fluoride ion to give the corresponding olefins in fairly good yields.Use of CsF in N,N-dimethylformamide gave the best result.
The Olefin Synthesis from β-Hydroxyalkylphosphonates Induced by Fluorides or Relatively Weak Bases
Kawashima, Takayuki,Ishii, Takafumi,Inamoto, Naoki,Tokitoh, Norihiro,Okazaki, Renji
, p. 209 - 219 (2007/10/03)
β-Hydroxyalkylphosphonates, which were prepared readily from alkylphosphonates and carbonyl compounds, were treated with a fluoride ion such as CsF or with relatively weak bases such as K2CO3 in N,N-dimethylformamide to give the corresponding olefins in good yields. One molar equivalent of water to bases is effective for increasing the yields of olefins. The stereochemistry of erythro-dimethyl (2-hydroxy-1-methyl-2-phenyl)ethylphosphonate was determined by X-ray crystallographic analysis. Use of threo-isomer gave (E)-olefin exclusively, while that of erythro-enricned isomer afforded predominantly (Z)-olefin, indicating that the present olefination proceeds stereospecifically in a manner of syn-elimination.
