bi(otf)3 and isoprene

bi(otf)3 has been researched along with isoprene* in 1 studies

Other Studies

1 other study(ies) available for bi(otf)3 and isoprene

Article	Year
Bi(OTf)3-catalysed prenylation of electron-rich aryl ethers and phenols with isoprene: a direct route to prenylated derivatives. Organic & biomolecular chemistry, 2011, Jul-21, Volume: 9, Issue:14 Electron-rich aryl ethers and phenols react with isoprene (2-methylbuta-1,3-diene) in the presence of catalytic Bi(OTf)(3) at 40 °C to afford the corresponding prenylated or 2,2-dimethylchroman products, respectively, in moderate to good yields. This transformation offers a convenient and expedient entry to prenylated derivatives of electron-rich aromatics that often display enhanced biological activities. The methodology has been employed in the efficient synthesis of a biologically active natural product and related compounds. Topics: Butadienes; Catalysis; Chromans; Electrons; Ethers; Hemiterpenes; Mesylates; Molecular Structure; Pentanes; Phenols; Prenylation; Stereoisomerism	2011

Article

Year

Bi(OTf)3-catalysed prenylation of electron-rich aryl ethers and phenols with isoprene: a direct route to prenylated derivatives.

Organic & biomolecular chemistry, 2011, Jul-21, Volume: 9, Issue:14

Electron-rich aryl ethers and phenols react with isoprene (2-methylbuta-1,3-diene) in the presence of catalytic Bi(OTf)(3) at 40 °C to afford the corresponding prenylated or 2,2-dimethylchroman products, respectively, in moderate to good yields. This transformation offers a convenient and expedient entry to prenylated derivatives of electron-rich aromatics that often display enhanced biological activities. The methodology has been employed in the efficient synthesis of a biologically active natural product and related compounds.

Topics: Butadienes; Catalysis; Chromans; Electrons; Ethers; Hemiterpenes; Mesylates; Molecular Structure; Pentanes; Phenols; Prenylation; Stereoisomerism

2011