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|Title:||Direct access to highly substituted 1-naphthols through palladium-catalyzed oxidative annulation of benzoylacetates and internal Alkynes||Authors:||Peng, S.
|Issue Date:||27-Sep-2013||Citation:||Peng, S., Wang, L., Wang, J. (2013-09-27). Direct access to highly substituted 1-naphthols through palladium-catalyzed oxidative annulation of benzoylacetates and internal Alkynes. Chemistry - A European Journal 19 (40) : 13322-13327. ScholarBank@NUS Repository. https://doi.org/10.1002/chem.201302740||Abstract:||One for the pot: 1-Naphthols, well-known structural design elements in medicinal chemistry, were readily prepared by means of a one-pot palladium-catalyzed oxidative annulation of readily available benzoylacetates to internal alkynes (see scheme). Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.||Source Title:||Chemistry - A European Journal||URI:||http://scholarbank.nus.edu.sg/handle/10635/93600||ISSN:||09476539||DOI:||10.1002/chem.201302740|
|Appears in Collections:||Staff Publications|
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