56207-33-1Relevant academic research and scientific papers
Room-temperature ionic liquid-promoted Williamson's synthesis of ethers: A facile synthesis of diaryloxymethanes
More,Ardhapure,Naik,Bhusare,Jadhav,Pawar
, p. 3113 - 3118 (2007/10/03)
A simple and efficient method has been developed for the synthesis of phenolic ethers using room-temperature ionic liquid, not only as solvent but also as promoter. Ionic liquid was recycled and subsequently reused without any loss of the product. Copyright Taylor & Francis, Inc.
Practical synthesis of diaryloxymethanes
Liu, Wenming,Szewczyk, Joanna,Waykole, Liladhar,Repic, Oljan,Blacklock, Thomas J.
, p. 1751 - 1754 (2007/10/03)
Diaryloxymethanes were prepared by treating phenols with sodium hydride and dichloromethane in N-methyl-pyrrolidinone (NMP) at 40°C.
Practical synthesis of diaryloxymethanes
Liu, Wenming,Szewczyk, Joanna,Waykole, Liladhar,Repic, Oljan,Blacklock, Thomas J.
, p. 2719 - 2723 (2007/10/03)
Diaryloxymethanes were prepared by treating phenols with sodium hydride and dichloromethane in N-methyl-pyrrolidinone (NMP) at 40°C.
Two new efficient preparations of enantiopure 2,2'-dihydroxy-6,6'-dimethoxyl-1,1'-biphenyl
Delogu, Giovanna,Fabbri, Davide
, p. 759 - 763 (2007/10/03)
Two new useful methods for the preparation of diol 1 starting from available compounds are described. Separation of the two enantiomers entails resolution of racemic diol 1 via the corresponding diastereomeric N-methylated phosphorothioamidates. Their separation by recrystallization followed by reduction afforded diol (aS)-1 and (aR)-1 in 100% and 72% ee, respectively.
