1364658-96-7Relevant academic research and scientific papers
Nickel-promoted highly regioselective carboxylation of aryl ynol ether and its application to the synthesis of chiral β-aryloxypropionic acid derivatives
Saito, Nozomi,Sun, Zhongdong,Sato, Yoshihiro
supporting information, p. 1170 - 1176 (2015/06/17)
Nickel(0)-promoted carboxylation of aryl ynol ether proceeded in a highly regioselective manner to produce α-substituted-β-aryloxyacrylic acid derivatives. The α-substituted-β-aryloxyacrylic acids were transformed into the corresponding β-aryloxypropionic
Copper-catalyzed coupling of 1,1-dibromo-1-alkenes with phenols: A general, modular, and efficient synthesis of ynol ethers, bromo enol ethers, and ketene acetals
Jouvin, Kevin,Bayle, Alexandre,Legrand, Frederic,Evano, Gwilherm
supporting information; experimental part, p. 1652 - 1655 (2012/06/05)
An efficient and general copper-catalyzed method is reported for the synthesis of phenol-derived 1-bromoenol ethers, ynol ethers, and ketene acetals by chemodivergent copper-catalyzed cross-coupling between readily available 1,1-dibromo-1-alkenes and phen
Copper-mediated selective cross-coupling of 1,1-dibromo-1-alkenes and heteronucleophiles: Development of general routes to heterosubstituted alkynes and alkenes
Jouvin, Kevin,Coste, Alexis,Bayle, Alexandre,Legrand, Frederic,Karthikeyan, Ganesan,Tadiparthi, Krishnaji,Evano, Gwilherm
, p. 7933 - 7947 (2013/01/16)
Efficient and general procedures for the cross-coupling of 1,1-dibromoalkenes and N-, O-, and P-nucleophiles are reported. Fine-tuning of the reaction conditions allows for either site-selective, double, or alkynylative cross-coupling, therefore providing
