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Regioselective Heck arylation of unsaturated alcohols by palladium catalysis in ionic liquid.
Chem Commun (Camb). 2006 Sep 14CC

Abstract

In contrast to almost all of the known examples of Heck arylation of unsaturated alcohols, which yield predominately beta-arylated products, arylation under the Pd-DPPP catalysis in ionic liquid leads preferentially to aryl substitution at the alpha carbon, providing an easy pathway to this valuable class of olefins.

Authors+Show Affiliations

Liverpool Center for Materials and Catalysis, Department of Chemistry, University of Liverpool, Liverpool, UK L69 7ZD.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

17047774

Citation

Mo, Jun, et al. "Regioselective Heck Arylation of Unsaturated Alcohols By Palladium Catalysis in Ionic Liquid." Chemical Communications (Cambridge, England), 2006, pp. 3591-3.
Mo J, Xu L, Ruan J, et al. Regioselective Heck arylation of unsaturated alcohols by palladium catalysis in ionic liquid. Chem Commun (Camb). 2006.
Mo, J., Xu, L., Ruan, J., Liu, S., & Xiao, J. (2006). Regioselective Heck arylation of unsaturated alcohols by palladium catalysis in ionic liquid. Chemical Communications (Cambridge, England), (34), 3591-3.
Mo J, et al. Regioselective Heck Arylation of Unsaturated Alcohols By Palladium Catalysis in Ionic Liquid. Chem Commun (Camb). 2006 Sep 14;(34)3591-3. PubMed PMID: 17047774.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Regioselective Heck arylation of unsaturated alcohols by palladium catalysis in ionic liquid. AU - Mo,Jun, AU - Xu,Lijin, AU - Ruan,Jiwu, AU - Liu,Shifang, AU - Xiao,Jianliang, Y1 - 2006/08/07/ PY - 2006/10/19/pubmed PY - 2007/5/22/medline PY - 2006/10/19/entrez SP - 3591 EP - 3 JF - Chemical communications (Cambridge, England) JO - Chem Commun (Camb) IS - 34 N2 - In contrast to almost all of the known examples of Heck arylation of unsaturated alcohols, which yield predominately beta-arylated products, arylation under the Pd-DPPP catalysis in ionic liquid leads preferentially to aryl substitution at the alpha carbon, providing an easy pathway to this valuable class of olefins. SN - 1359-7345 UR - https://www.unboundmedicine.com/medline/citation/17047774/Regioselective_Heck_arylation_of_unsaturated_alcohols_by_palladium_catalysis_in_ionic_liquid_ L2 - https://doi.org/10.1039/b608033b DB - PRIME DP - Unbound Medicine ER -