DOI: 10.1055/s-00000084

Synthesis

Issue 24 · Volume 2008 · December 2008 DOI: 10.1055/s-002-13961

review

  • 3877
  • paper

  • 3903
    Kérourédan, Erwan; Percy, Jonathan M.; Rinaudo, Giuseppe; Singh, Kuldip:

    A Concise Route to Difluorinated Analogues of Cyclitols and Sugars

    Image for article: A Concise Route to Difluorinated
Analogues of Cyclitols and Sugars
  • 3919
    Sun, Lili; Peng, Guisheng; Niu, Hongmei; Wang, Qiang; Li, Chunbao:

    A Highly Chemoselective and Rapid Chlorination of Benzyl Alcohols under Neutral Conditions

    Image for article: A Highly Chemoselective and
Rapid Chlorination of Benzyl Alcohols under Neutral Conditions
  • 3925
  • 3931
  • 3937
    Nieddu, Giammario; De Luca, Lidia; Giacomelli, Giampaolo:

    A Chemoselective, Easy Bromination of (Hydroxymethyl)phenols

    Image for article: A Chemoselective, Easy Bromination
of (Hydroxymethyl)phenols
  • 3941
  • 3945
    Yadav, J. S.; Ather, Hissana; Gayathri, K. Uma; Rao, N. Venkateswar; Prasad, A. R.:

    Stereoselective Formal Synthesis of Herbarumin III via Prins Cyclization

    Image for article: Stereoselective Formal Synthesis
of Herbarumin III via Prins Cyclization
  • 3951
  • 3957
    Gurba, Patrice; Vallinayagam, Ramakrishnan; Schmitt, Frédéric; Furrer, Julien; Juillerat-Jeanneret, Lucienne; Neier, Reinhard:

    Novel Bioconjugates of Aminolevulinic Acid with Nucleosides

    Image for article: Novel Bioconjugates of Aminolevulinic
Acid with Nucleosides
  • 3963
  • 3967
  • 3974
    Zhou, Jing; Fu, Liangbing; Lv, Man; Liu, Jinsong; Pei, Duanqing; Ding, Ke:

    Copper(I) Iodide Catalyzed Domino Process to Quinazolin-4(3H)-ones

    Image for article: Copper(I) Iodide Catalyzed Domino
Process to Quinazolin-4(3<EM EMTYPE="ITALIC">H</EM>)-ones
  • 3981
  • 3988
  • 3995
  • 4002
  • 4007
    Kalinski, Cédric; Lemoine, Hugues; Schmidt, Jürgen; Burdack, Christoph; Kolb, Jürgen; Umkehrer, Michael; Ross, Günther:

    Multicomponent Reactions as a Powerful Tool for Generic Drug Synthesis

    Image for article: Multicomponent Reactions as
a Powerful Tool for Generic Drug Synthesis
  • 4012
    Nagl, Michael; Panuschka, Claudia; Barta, Andrea; Schmid, Walther:

    The BF3×OEt2-Assisted Conversion of Nitriles into Thioamides with Lawesson’s Reagent

    Image for article: The BF<SUB>3</SUB>×OEt<SUB>2</SUB>-Assisted
Conversion of Nitriles into Thioamides with Lawesson’s
Reagent
  • 4019
    Alvarez-Manzaneda, Enrique; Chahboun, Rachid; Cabrera, Eduardo; Alvarez, Esteban; Haidour, Ali; Ramos, Jose Miguel; Alvarez-Manzaneda, Ramón; Romera, Juan Luis; Escobar, Mari Angeles; Messouri, Ibtissam:

    A New Synthetic Strategy towards Bioactive Merosesquiterpenoids

    Image for article: A New Synthetic Strategy towards
Bioactive Merosesquiterpenoids
  • 4028
    Gryko, Daniel T.; Wyrostek, Dagmara; Nowak-Król, Agnieszka; Abramczyk, Katarzyna; Rogacki, Maciej K.:

    Straightforward Transformation of Pentafluorobenzaldehyde into 4-Aryloxy-2,3,5,6-tetrafluorobenzaldehydes

    Image for article: Straightforward Transformation
of Pentafluorobenzaldehyde into 4-Aryloxy-2,3,5,6-tetrafluorobenzaldehydes
  • practical synthetic procedures

  • 4033
    L’Helgoual’ch, Jean-Martial; Bentabed-Ababsa, Ghenia; Chevallier, Floris; Derdour, Aïcha; Mongin, Florence:

    Synthesis of 2,5-Diiodopyrazine by Deprotonative Dimetalation of Pyrazine

    Image for article: Synthesis of 2,5-Diiodopyrazine
by Deprotonative Dimetalation of Pyrazine
  • 4036