Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/94631
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dc.contributor.authorXing, Chongen
dc.contributor.authorSun, Huien
dc.contributor.authorZhang, Junminen
dc.contributor.authorLi, Guohuien
dc.contributor.authorChi, Robin Yongguien
dc.date.accessioned2012-05-22T09:10:43Zen
dc.date.accessioned2019-12-06T18:59:29Z-
dc.date.available2012-05-22T09:10:43Zen
dc.date.available2019-12-06T18:59:29Z-
dc.date.copyright2011en
dc.date.issued2011en
dc.identifier.citationXing, C., Sun, H., Zhang, J., Li, G. & Chi, R. Y. (2011). Brønsted Acid Catalyzed α-Alkylation of Aldehydes with Diaryl Methyl Alcohols. Chemistry - A European Journal, 17(44), 12272-12275.en
dc.identifier.urihttps://hdl.handle.net/10356/94631-
dc.identifier.urihttp://hdl.handle.net/10220/8118en
dc.description.abstractA proton does the two jobs: Brønsted acids alone catalyze the α-alkylation of aldehydes with diaryl alcohols. In this type of transformation, the acid-catalysis approach offers a broader substrate scope compared to the previously used enamine catalysis methods. The acid plays two important roles: one is to mediate the alcohol dehydration for carbocation formation; the other is to accelerate the rate-determining aldehyde enolization.en
dc.language.isoenen
dc.relation.ispartofseriesChemistry - a European journalen
dc.rights© 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.en
dc.titleBrønsted acid catalyzed α-alkylation of aldehydes with diaryl methyl alcoholsen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doihttp://dx.doi.org/10.1002/chem.201102623en
dc.identifier.rims165054en
item.grantfulltextnone-
item.fulltextNo Fulltext-
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