139016-15-2Relevant academic research and scientific papers
Phenol and aniline oxidative coupling with alkenes by using hypervalent iodine dimer for the rapid access to dihydrobenzofurans and indolines
Dohi, Toshifumi,Toyoda, Yosuke,Nakae, Tomofumi,Koseki, Daichi,Kubo, Hiroko,Kamitanaka, Tohru,Kita, Yasuyuki
, p. 631 - 644 (2015)
A highly reactive hypervalent iodine dimer, [Ph(CF3COO)I]-O- [I(OCOCF3)Ph], is utilized as successful promoter in the oxidative phenolic coupling with styrenes leading to 2-aryldihydrobenzofurans. The extensions of the substrates in this study have led to the development of a new expeditious construction of the pyrroloindoline structure from aniline and enamide derivatives.
Mechanistic Aspects and Synthetic Applications of the Electrochemical and Iodobenzene Bis(trifluoroacetate) Oxidative 1,3-Cycloadditions of Phenols and Electron-Rich Styrene Derivatives
Gates, Bradley D.,Dalidowicz, Peter,Tebben, Andrew,Wang, Shaopeng,Swenton, John S.
, p. 2135 - 2143 (2007/10/02)
Anodic oxidation of p-methoxy-substituted phenols and electron-rich styrene or propenylbenzene derivatives affords in good yield trans-dihydrobenzofurans derived from a formal 1,3-oxidative cycloaddition of the phenol to the styrene derivative.The yield o
