4790-71-0Relevant articles and documents
Development and Mechanistic Study of Quinoline-Directed Acyl C-O Bond Activation and Alkene Oxyacylation Reactions
Hoang, Giang T.,Walsh, Dylan J.,McGarry, Kathryn A.,Anderson, Constance B.,Douglas, Christopher J.
, p. 2972 - 2983 (2017/03/23)
The intramolecular addition of both an alkoxy and acyl substituent across an alkene, oxyacylation of alkenes, using rhodium catalyzed C-O bond activation of an 8-quinolinyl ester is described. Our unsuccessful attempts at intramolecular carboacylation of ketones via C-C bond activation ultimately informed our choice to pursue and develop the intramolecular oxyacylation of alkenes via quinoline-directed C-O bond activation. We provide a full account of our catalyst discovery, substrate scope, and mechanistic experiments for quinoline-directed alkene oxyacylation.
Method for preparing o-methallyloxyphenol
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Paragraph 0038; 0045, (2016/11/28)
The invention provides a method for preparing o-methallyloxyphenol. According to the method, catechol and 3-chloro-2-methylpropene serving as raw materials are catalyzed under specific solvent, acid-binding agent, catalyst and proper reaction condition to
PURIFICATION PROCESS FOR PARA-METHALLYLPYROCATECHOL
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Page/Page column 2; 7-8, (2013/02/28)
The present invention relates to a process for the purification of para-methallylpyrocatechol and to the preparation of flavor and fragrance compounds from para-methallylpyrocatechol.