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Copper catalyzed arylation/C-C bond activation: an approach toward alpha-aryl ketones.
J Am Chem Soc. 2010 Jun 23; 132(24):8273-5.JA

Abstract

An efficient arylation/C-C activation process was discovered. Beta-diketones with aryl halides (aryl iodides and aryl bromides) could undergo reaction smoothly in the presence of Cu(I) or Cu(II) salts in DMSO using K(3)PO(4) x 3 H(2)O without ligands. The role of H(2)O was unprecedented, which assisted the C-C activation. Various alpha-aryl ketones could be efficiently synthesized by this novel method. In situ monitoring of the formation of KOAc and experimentation relating to "a classic diagnostic technique for the participation of radical anion intermediates" revealed the preliminary mechanistic information for the reaction. This method is simple, general, and practical which complemented the classic method for the rapid construction of C-C bonds to a carbonyl moiety.

Authors+Show Affiliations

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072, PR China.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

20518466

Citation

He, Chuan, et al. "Copper Catalyzed arylation/C-C Bond Activation: an Approach Toward Alpha-aryl Ketones." Journal of the American Chemical Society, vol. 132, no. 24, 2010, pp. 8273-5.
He C, Guo S, Huang L, et al. Copper catalyzed arylation/C-C bond activation: an approach toward alpha-aryl ketones. J Am Chem Soc. 2010;132(24):8273-5.
He, C., Guo, S., Huang, L., & Lei, A. (2010). Copper catalyzed arylation/C-C bond activation: an approach toward alpha-aryl ketones. Journal of the American Chemical Society, 132(24), 8273-5. https://doi.org/10.1021/ja1033777
He C, et al. Copper Catalyzed arylation/C-C Bond Activation: an Approach Toward Alpha-aryl Ketones. J Am Chem Soc. 2010 Jun 23;132(24):8273-5. PubMed PMID: 20518466.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Copper catalyzed arylation/C-C bond activation: an approach toward alpha-aryl ketones. AU - He,Chuan, AU - Guo,Sheng, AU - Huang,Li, AU - Lei,Aiwen, PY - 2010/6/4/entrez PY - 2010/6/4/pubmed PY - 2010/6/4/medline SP - 8273 EP - 5 JF - Journal of the American Chemical Society JO - J Am Chem Soc VL - 132 IS - 24 N2 - An efficient arylation/C-C activation process was discovered. Beta-diketones with aryl halides (aryl iodides and aryl bromides) could undergo reaction smoothly in the presence of Cu(I) or Cu(II) salts in DMSO using K(3)PO(4) x 3 H(2)O without ligands. The role of H(2)O was unprecedented, which assisted the C-C activation. Various alpha-aryl ketones could be efficiently synthesized by this novel method. In situ monitoring of the formation of KOAc and experimentation relating to "a classic diagnostic technique for the participation of radical anion intermediates" revealed the preliminary mechanistic information for the reaction. This method is simple, general, and practical which complemented the classic method for the rapid construction of C-C bonds to a carbonyl moiety. SN - 1520-5126 UR - https://www.unboundmedicine.com/medline/citation/20518466/Copper_catalyzed_arylation/C_C_bond_activation:_an_approach_toward_alpha_aryl_ketones_ L2 - https://doi.org/10.1021/ja1033777 DB - PRIME DP - Unbound Medicine ER -
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