1638643-98-7Relevant academic research and scientific papers
Synthesis of N-substituted (Z)-3-arylbenzo[c]thiophen1(3H)-imines by the reaction of 1-[aryl(methoxy)methyl]2-lithiobenzenes with isothiocyanates followed by acid-mediated cyclization
Kobayashi, Kazuhiro,Shigemura, Yuuho,Ezaki, Kosuke
, p. 526 - 536 (2015)
A simple procedure for the preparation of N-substituted (Z)-3-arylbenzo [c]thiophen-1(3H)-imines has been developed. Thus, bromine/lithium exchange between 1-[aryl(methoxy)methyl]-2-bromobenzenes and butyllithium, followed by reaction of the resulting 1-[
Synthesis of substituted biaryls through gold-catalyzed petasis-ferrier rearrangement of propargyl ethers
Pati, Kamalkishore,Alabugin, Igor V.
supporting information, 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
