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Direct access to highly substituted 1-naphthols through palladium-catalyzed oxidative annulation of benzoylacetates and internal alkynes.
Chemistry. 2013 Sep 27; 19(40):13322-7.C

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.

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Publisher Full Text (DOI)

Authors+Show Affiliations

Peng S
Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543 (Singapore), Fax: (+65) 6516-1691.
Wang L
No affiliation info available
Wang J
No affiliation info available

MeSH

AlkynesBenzoatesCatalysisMolecular StructureNaphtholsOxidation-ReductionPalladium

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

24078414

Citation

Peng, Shiyong, et al. "Direct Access to Highly Substituted 1-naphthols Through Palladium-catalyzed Oxidative Annulation of Benzoylacetates and Internal Alkynes." Chemistry (Weinheim an Der Bergstrasse, Germany), vol. 19, no. 40, 2013, pp. 13322-7.
Peng S, Wang L, Wang J. Direct access to highly substituted 1-naphthols through palladium-catalyzed oxidative annulation of benzoylacetates and internal alkynes. Chemistry. 2013;19(40):13322-7.
Peng, S., Wang, L., & Wang, J. (2013). Direct access to highly substituted 1-naphthols through palladium-catalyzed oxidative annulation of benzoylacetates and internal alkynes. Chemistry (Weinheim an Der Bergstrasse, Germany), 19(40), 13322-7. https://doi.org/10.1002/chem.201302740
Peng S, Wang L, Wang J. Direct Access to Highly Substituted 1-naphthols Through Palladium-catalyzed Oxidative Annulation of Benzoylacetates and Internal Alkynes. Chemistry. 2013 Sep 27;19(40):13322-7. PubMed PMID: 24078414.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Direct access to highly substituted 1-naphthols through palladium-catalyzed oxidative annulation of benzoylacetates and internal alkynes. AU - Peng,Shiyong, AU - Wang,Lei, AU - Wang,Jian, PY - 2013/07/14/received PY - 2013/10/1/entrez PY - 2013/10/1/pubmed PY - 2014/6/11/medline KW - CH activation KW - alkynes KW - annulation KW - naphthols KW - palladium SP - 13322 EP - 7 JF - Chemistry (Weinheim an der Bergstrasse, Germany) JO - Chemistry VL - 19 IS - 40 N2 - 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. SN - 1521-3765 UR - https://www.unboundmedicine.com/medline/citation/24078414/Direct_access_to_highly_substituted_1_naphthols_through_palladium_catalyzed_oxidative_annulation_of_benzoylacetates_and_internal_alkynes_ L2 - https://doi.org/10.1002/chem.201302740 DB - PRIME DP - Unbound Medicine ER -