Direct access to highly substituted 1-naphthols through palladium-catalyzed oxidative annulation of benzoylacetates and internal Alkynes

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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