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Search for "nitrogen heterocycles" in Full Text gives 79 result(s) in Beilstein Journal of Organic Chemistry.

Approaches towards the synthesis of 5-aminopyrazoles

  • Ranjana Aggarwal,
  • Vinod Kumar,
  • Rajiv Kumar and
  • Shiv P. Singh

Beilstein J. Org. Chem. 2011, 7, 179–197, doi:10.3762/bjoc.7.25

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  • -dielectrophiles has been extensively used for the preparation of bicyclic nitrogen heterocycles, especially in the preparation of condensed heterocycles such as pyrazolo[3,4-d]pyrimidines, pyrazolo[3,4-b]pyridines, imidazopyrazoles etc. In view of significant interest in the synthesis of these heterocyclics, we
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Published 09 Feb 2011

EPR and pulsed ENDOR study of intermediates from reactions of aromatic azides with group 13 metal trichlorides

  • Giorgio Bencivenni,
  • Riccardo Cesari,
  • Daniele Nanni,
  • Hassane El Mkami and
  • John C. Walton

Beilstein J. Org. Chem. 2010, 6, 713–725, doi:10.3762/bjoc.6.84

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  • ], and δ-azidoesters and chlorides into allylated nitrogen heterocycles [30]. To help in elucidating the mechanisms of these reductions, we used CW EPR spectroscopy and attempted to characterise the reactive intermediates in selected reactions involving gallium trichloride. Surprisingly, we found that
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Published 09 Aug 2010

Development of potential manufacturing routes for substituted thiophenes – Preparation of halogenated 2-thiophenecarboxylic acid derivatives as building blocks for a new family of 2,6-dihaloaryl 1,2,4-triazole insecticides

  • John W. Hull Jr.,
  • Duane R. Romer,
  • David E. Podhorez,
  • Mezzie L. Ash and
  • Christine H. Brady

Beilstein J. Org. Chem. 2007, 3, No. 23, doi:10.1186/1860-5397-3-23

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  • ). [22][23] The vapor phase chlorination of nitrogen heterocycles has been reported. [22] The analogous vapor phase chlorination of thiophene 20 was carried out in the present study using a down flow quartz reactor tube heated with an electric furnace to high temperatures, and filled with an inert
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Published 04 Sep 2007

An efficient synthesis of tetramic acid derivatives with extended conjugation from L-Ascorbic Acid

  • Biswajit K. Singh,
  • Surendra S. Bisht and
  • Rama P. Tripathi

Beilstein J. Org. Chem. 2006, 2, No. 24, doi:10.1186/1860-5397-2-24

Graphical Abstract
  • antibiotics and thus this method offers a new and short route for the synthesis of tetramic acid derivatives of biological significance. 1. Background Tetramic acid derivatives constitute an important class of nitrogen heterocycles with pyrrolidine-2,4-dione moieties and are key structural motifs in many
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Published 06 Dec 2006
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