These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

272 related items for PubMed ID: 20843092

  • 1. Hofmann rearrangement of carboxamides mediated by hypervalent iodine species generated in situ from iodobenzene and oxone: reaction scope and limitations.
    Zagulyaeva AA, Banek CT, Yusubov MS, Zhdankin VV.
    Org Lett; 2010 Oct 15; 12(20):4644-7. PubMed ID: 20843092
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Catalytic hypervalent iodine oxidation using 4-iodophenoxyacetic acid and oxone: oxidation of p-alkoxyphenols to p-benzoquinones.
    Yakura T, Tian Y, Yamauchi Y, Omoto M, Konishi T.
    Chem Pharm Bull (Tokyo); 2009 Mar 15; 57(3):252-6. PubMed ID: 19252315
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Synthesis of tetrahydropyrroloiminoquinone alkaloids based on electrochemically generated hypervalent iodine oxidative cyclization.
    Inoue K, Ishikawa Y, Nishiyama S.
    Org Lett; 2010 Feb 05; 12(3):436-9. PubMed ID: 20039698
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Hypervalent iodine-catalyzed oxylactonization of ketocarboxylic acids to ketolactones.
    Uyanik M, Yasui T, Ishihara K.
    Bioorg Med Chem Lett; 2009 Jul 15; 19(14):3848-51. PubMed ID: 19376702
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. An effective and catalytic oxidation using recyclable fluorous IBX.
    Miura T, Nakashima K, Tada N, Itoh A.
    Chem Commun (Camb); 2011 Feb 14; 47(6):1875-7. PubMed ID: 21127797
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Hypervalent iodine reagents as a new entrance to organocatalysts.
    Dohi T, Kita Y.
    Chem Commun (Camb); 2009 Apr 28; (16):2073-85. PubMed ID: 19360157
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Reactivity of hydroxy- and aquo(hydroxy)-λ3-iodane-crown ether complexes.
    Miyamoto K, Yokota Y, Suefuji T, Yamaguchi K, Ozawa T, Ochiai M.
    Chemistry; 2014 Apr 25; 20(18):5447-53. PubMed ID: 24644216
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.