Please use this identifier to cite or link to this item: https://doi.org/10.1002/chem.201302740
Title: Direct access to highly substituted 1-naphthols through palladium-catalyzed oxidative annulation of benzoylacetates and internal Alkynes
Authors: Peng, S.
Wang, L.
Wang, J. 
Keywords: alkynes
annulation
C-H activation
naphthols
palladium
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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