55075-32-6Relevant academic research and scientific papers
(III) a Sc catalyzes mellowly to the in-situ formation of O-methylene benzoquinone oxa Michael addition reaction method (by machine translation)
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Paragraph 0023, (2019/04/06)
The present invention provides a Sc (III) catalyzes mellowly to the in-situ formation of O-methylene benzoquinone oxa Michael addition reaction method, in order to 2 - (hydroxy (phenyl) methyl) phenol compound and alcohol compound (III) by the Sc catalyti
Mannich Bases, XXI: Exchange Reactions of Phenolic Mannich Bases
Moehrle, Hans,Miller, Christoph
, p. 229 - 236 (2007/10/02)
Various p-substituted phenolic Mannich bases (and to a minor degree o-substituted derivatives) form alcohols and ethers when heated in aqueous alcohols in the presence of Na2EDTA or acetic acid.The reaction proceeds with amine elimination and subsequent addition of the solvent to the resulting quinone methide.
