Solid-Phase synthesis of aryl vinyl ethers based on polystyrenesupported aβ-phenylselenoethanol
A novel facile solid-phase organic synthesis of aryl vinyl ethers by reaction of polystyrene-supported β-phenylselenoethanol with phenols under Mitsunobu conditions and subsequent oxidation-elimination with 30% hydrogen peroxide has been developed. The ad
β-Phenylselenoethanol, an efficient reagent for the one-pot synthesis of aryl vinyl ethers
β-Phenylselenoethanol was treated with phenols under Mitsunobu conditions and subsequent oxidation-elimination with 30% hydrogen peroxide furnished aryl vinyl ethers with good yields (85-90%) in a one-pot, two-step transformation.
Fu, Gui-Yun,Yu, La-Mei,Mao, Xue-Chun,Wu, Dan
experimental part
p. 595 - 597
(2009/10/15)
Iridium-catalyzed synthesis of vinyl ethers from alcohols and vinyl acetate
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Hirabayashi, Tomotaka,Sakaguchi, Satoshi,Ishii, Yasutaka,Davies, Paul W.,Fürstner, Alois
p. 55 - 58
(2017/09/25)
Polymer-supported β-bromoethyl selenide: An efficient reagent for the synthesis of aryl vinyl ethers
A simple and efficient procedure for the solid-phase synthesis of aryl vinyl ethers using polymer-supported β-bromoethyl selenide with traceless linker strategy is described.