1638643-95-4Relevant articles and documents
Synthesis of substituted biaryls through gold-catalyzed petasis-ferrier rearrangement of propargyl ethers
Pati, Kamalkishore,Alabugin, Igor V.
, p. 3986 - 3990 (2014/07/08)
Au-catalyzed cycloisomerization of aryl propargyl ethers provides controlled transition from alkyne to carbonyl chemistry followed up by a Petasis-Ferrier rearrangement/aromatization cascade leading to substituted biaryls with functionalized naphthalene cores. An Au-catalyzed sequence of alkoxy group translocation, Petasis-Ferrier rearrangement, and aromatization transforms aryl propargyl ethers into substituted biaryls with functionalized naphthalene cores. Copyright
