化学
羟基化
催化作用
芳基
水介质
组合化学
有机化学
水溶液
硼酸
绿色化学
反应机理
烷基
酶
作者
Sai Srinivas Ponugoti,Rutuja S. Vibuthe,Sandip J. Detke,Prashant S. Kharkar,Shreerang V. Joshi
标识
DOI:10.1080/00397911.2023.2203826
摘要
AbstractA highly efficient protocol was developed for the ipso hydroxylation of arylboronic acids using citric acid as an effective organocatalyst. The sustainable methodology offers good to excellent yields with in the rapid reaction time in water as a solvent media and 30% H2O2 as an oxidant. The reaction proceeds without the aid of any metal catalyst or base and is simple, safe, and clean. The current protocol enables the access to variety of phenols and is found to be tolerable to the diverse electronic substrates. Even, the devised reaction conditions have been found to be effective in the gram-scale synthesis of an API, Mequinol.Keywords: Arylboronic acidsipso hydroxylationmetal-freeorganocatalyzed AcknowledgmentsThe authors are thankful to the Department of Pharmaceutical Sciences and Technology, ICT-Mumbai for providing all the facilities.Disclosure statementNo potential conflict of interest was reported by the author(s).
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