DOI: 10.1055/s-00000084

Synthesis

Issue 21 · Volume 2010 · November 2010 DOI: 10.1055/s-002-21424

synform

  • A86
  • review

  • 3583
  • practical synthetic procedures

  • 3596
  • paper

  • 3602
  • 3609
    Higuchi, Kazuhiro; Saito, Keita; Hirayama, Tetsuya; Watanabe, Yoshiaki; Kobayashi, Emiko; Kawasaki, Tomomi:

    Claisen Rearrangement through Enolization of 2-Allyloxyindolin-3-ones: Construction of Adjacent Carbon Stereocenters in 3-Hydroxyindolin-2-ones

    Image for article: Claisen Rearrangement through
Enolization of 2-Allyloxyindolin-3-ones: Construction
of Adjacent Carbon Stereocenters in 3-Hydroxyindolin-2-ones
  • 3615
  • 3623
  • 3627
  • 3631
    Bergeron, Raymond J.; Singh, Shailendra; Bharti, Neelam; Jiang, Yi:

    Design, Synthesis, and Testing of Polyamine Vectored Iron Chelators

    Image for article: Design, Synthesis, and Testing
of Polyamine Vectored Iron Chelators
  • 3637
    Vyvyan, James R.; Dell, Jennifer A.; Ligon, Toby J.; Motanic, Kelsey K.; Wall, Hayley S.:

    Suzuki-Miyaura Cross-Coupling of 3-Pyridyl Triflates with Alk-1-enyl-2-pinacol Boronates

    Image for article: Suzuki-Miyaura Cross-Coupling
of 3-Pyridyl Triflates with Alk-1-enyl-2-pinacol Boronates
  • 3645
  • 3649
    Rajan, Rani; John, Jubi; Thulasi, Sreeja; Joseph, Nayana; Radhakrishnan, K. V.; Sawant, R. C.:

    Trapping the π-Allylpalladium Intermediate from Fulvene-Derived Azabicyclic Olefin with Soft Nucleophiles

    Image for article: Trapping the π-Allylpalladium
Intermediate from Fulvene-Derived Azabicyclic Olefin with
Soft Nucleophiles
  • 3657
    Yadav, Jhillu S.; Thrimurtulu, N.; Rahman, Md. Ataur; Reddy, J. Satyanarayana; Prasad, A. R.; Reddy, B. V. Subba:

    Stereoselective Total Synthesis of (3R,5R)-5-Hydroxy-de-O-methyllasiodiplodin via the Prins Cyclization

    Image for article: Stereoselective Total Synthesis
of (3<EM EMTYPE="ITALIC">R</EM>,5<EM EMTYPE="ITALIC">R</EM>)-5-Hydroxy-de-<EM EMTYPE="ITALIC">O</EM>-methyllasiodiplodin via the Prins Cyclization
  • 3663
  • 3670
  • 3681
    Yusubov, Mehman S.; Yusubova, Rosa Y.; Funk, Tatyana V.; Chi, Ki-Whan; Kirschning, Andreas; Zhdankin, Viktor V.:

    m-Iodosylbenzoic Acid as a Convenient Recyclable Hypervalent Iodine Oxidant for the Synthesis of α-Iodo Ketones by Oxidative Iodination of Ketones

    Image for article: <EM EMTYPE="ITALIC">m</EM>-Iodosylbenzoic
Acid as a Convenient Recyclable Hypervalent Iodine Oxidant for the
Synthesis of α-Iodo Ketones by Oxidative Iodination of
Ketones
  • 3686
  • 3693
  • 3700
    Nieto, Elena; Alajarín, Ramón; Álvarez-Builla, Julio; Larrañaga, Ignacio; Gorospe, Elena; Pozo, Miguel A.:

    A New and Improved Synthesis of the Precursor of the Hypoxia Marker [¹8F]-FMISO

    Image for article: A New and Improved Synthesis
of the Precursor of the Hypoxia Marker [<SUP>¹8</SUP>F]-FMISO
  • 3705
  • 3710
    Chandrasekhar, Srivari; Srihari, Pabbaraja; Nagesh, Chidalla; Kiranmai, Nayani; Nagesh, Narayana; Idris, M. Mohammed:

    Synthesis of Readily Accessible Triazole-Linked Dimer Deoxynucleoside Phosphoramidite for Solid-Phase Oligonucleotide Synthesis

    Image for article: Synthesis of Readily Accessible
Triazole-Linked Dimer Deoxynucleoside Phosphoramidite
for Solid-Phase Oligonucleotide Synthesis
  • 3715
  • 3724
    Artem’ev, Alexander V.; Gusarova, Nina K.; Malysheva, Svetlana F.; Kraikivskii, Peter B.; Belogorlova, Nataliya A.; Trofimov, Boris A.:

    Efficient General Synthesis of Alkylammonium Diselenophosphinates via Multicomponent One-Pot Reaction of Secondary Phosphines with Elemental Selenium and Amines

    Image for article: Efficient General Synthesis
of Alkylammonium Diselenophosphinates via Multicomponent One-Pot
Reaction of Secondary Phosphines with Elemental Selenium and Amines
  • 3731
    Das, Biswanath; Reddy, Cheruku Ravindra; Sindhu, Chava; Sudhakar, Chithaluri; Nagendra, Siddavatam:

    Friedel-Crafts Reactions of 2-Naphthol with α-Amido Sulfones and Conversion of the Products with Nucleophiles

    Image for article: Friedel-Crafts Reactions
of 2-Naphthol with α-Amido Sulfones and Conversion
of the Products with Nucleophiles
  • 3736
  • 3741
  • 3745
  • 3755
  • addenda and errata

  • 3761
  • 3762
  • e5