68299-87-6Relevant academic research and scientific papers
Unusual transformation of 4-hydroxy/methoxybenzylic alcohols via C[sbnd]C ipso-substitution reaction using proton-exchanged montmorillonite as media
Chen, Dongyin,Chen, Xuan,Dong, Zezhong,Jiang, Nan,Li, Fei,Yun, Yangfang,Zhou, Yu
supporting information, (2020/11/12)
We present here proton-exchanged montmorillonite-mediated an unusual transformation of 4-hydroxy and 4-methoxybenzylic alcohols to form symmetrical benzylic ethers and diarylmethanes under mild conditions. Nuclear magnetic resonance spectroscopy and density functional theory calculations support a plausible mechanism, which includes a distinctive aromatic C[sbnd]C ipso-substitution reaction with a hydroxymethyl group as the C-based leaving group.
Cyclic and linear oligomerization reaction of 3,4,5-trimethoxybenzyl alcohol with a bentonite-clay
Salmon, Manuel,Zavala, Nieves,Martinez, Mariano,Miranda, Rene,Cruz, Raymundo,Cardenas, Jorge,Gavino, Ruben,Cabrera, Armando
, p. 5797 - 5800 (2007/10/02)
The catalytic induction and structures of cyclic and linear oligomers from 3,4,5-trimethoxybenzyl alcohol with a bentonite clay as catalyst are discussed.
