54384-75-7Relevant articles and documents
Rhodium-catalyzed synthesis of esters from aryl iodides and alcohols: use of alcohols with/without the assistance of aldehydes as carbon monoxide and nucleophile sources
Kim, Ju Hyun,Park, Hawon,Chung, Young Keun
, p. 190 - 194 (2017/01/12)
A CO-gas-free rhodium-catalyzed alkoxycarbonylation of aryl iodide with alcohols has been developed. Alcohols, with/without the aid of an aldehyde, were used as a carbon monoxide and nucleophile source. The former synthesis afforded better yields of the alkoxycarbonylated products. Moreover, phenols also afforded phenoxycarbonylation products with high yields.
Zeolite-mediated conversion of alcohols to p-methoxybenzyl ethers
Sharma,Punna, Sreenivas,Ratnamala,Durga Kumari,Subrahmanyam
, p. 581 - 586 (2007/10/03)
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Mechanism of Anodic Cleavage of Benzyl Ethers
Boyd, Jean W.,Schmalzl, Paul W.,Miller, Larry L.
, p. 3856 - 3862 (2007/10/02)
Kinetic isotope effects and substituent effects are utilized to elucidate the mechanism of the anodic oxidation of benzyl ethers at platinum in acetonitrile.All of the data, including some previously published results, are consistent with a mechanism involving phenylalkoxy carbonium ions.Much of the data is incompatible with a previous mechanistic proposal involving initial oxidative cleavage of the benzyl carbon-oxygen bond.
