Chemical templates

  1. editorImage
  1. Editor: Prof. Sigurd Höger
    Rheinische Friedrich-Wilhelms-Universität Bonn

A chemical template controls a reaction in such a way that from a multitude of possible products a specific one is preferentially or even exclusively formed. The template can influence the reaction in a stoichiometric or a catalytic way, it can be reused or remain in the product as an integral part. Remarkable breakthroughs in synthetic, spectroscopic and microscopic as well as theoretical methods facilitate a closer investigation and more detailed understanding of template effects in all areas of chemistry. It will also lead to the identification of new template effects and new methodologies for the adaptation of existing binding motifs into functional chemical matrices. The articles in this Thematic Series represent a snapshot of the current activities in template-directed reactions. This selection from a broad variety of different fields of chemistry will hopefully be inspiring for the reader, thus leading to new exciting discoveries in template chemistry and attract new audience to this field.

See also the Thematic Series:
Superstructures with cyclodextrins: Chemistry and applications IV
Supramolecular chemistry at the interface of biology, materials and medicine

Chemical templates

  1. Sigurd Höger
  • Editorial
  • Published 22 Jul 2014

Beilstein J. Org. Chem. 2014, 10, 1670–1671, doi:10.3762/bjoc.10.174

Novel supramolecular affinity materials based on (−)-isosteviol as molecular templates

  1. Christina Lohoelter,
  2. Malte Brutschy,
  3. Daniel Lubczyk and
  4. Siegfried R. Waldvogel
  • Full Research Paper
  • Published 09 Dec 2013

  • PDF

  • Supp. Info

Beilstein J. Org. Chem. 2013, 9, 2821–2833, doi:10.3762/bjoc.9.317

Self-assembly of metallosupramolecular rhombi from chiral concave 9,9’-spirobifluorene-derived bis(pyridine) ligands

  1. Rainer Hovorka,
  2. Sophie Hytteballe,
  3. Torsten Piehler,
  4. Georg Meyer-Eppler,
  5. Filip Topić,
  6. Kari Rissanen,
  7. Marianne Engeser and
  8. Arne Lützen
  • Full Research Paper
  • Published 18 Feb 2014

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  • Supp. Info

Beilstein J. Org. Chem. 2014, 10, 432–441, doi:10.3762/bjoc.10.40

  • Full Research Paper
  • Published 09 Apr 2014

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  • Supp. Info

Beilstein J. Org. Chem. 2014, 10, 814–824, doi:10.3762/bjoc.10.77

  • Full Research Paper
  • Published 09 Apr 2014

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  • Supp. Info

Beilstein J. Org. Chem. 2014, 10, 825–831, doi:10.3762/bjoc.10.78

  • Full Research Paper
  • Published 23 Apr 2014

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  • Supp. Info

Beilstein J. Org. Chem. 2014, 10, 910–920, doi:10.3762/bjoc.10.89

Substitution effect and effect of axle’s flexibility at (pseudo-)rotaxanes

  1. Friedrich Malberg,
  2. Jan Gerit Brandenburg,
  3. Werner Reckien,
  4. Oldamur Hollóczki,
  5. Stefan Grimme and
  6. Barbara Kirchner
  • Full Research Paper
  • Published 05 Jun 2014

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  • Supp. Info

Beilstein J. Org. Chem. 2014, 10, 1299–1307, doi:10.3762/bjoc.10.131

Triazol-substituted titanocenes by strain-driven 1,3-dipolar cycloadditions

  1. Andreas Gansäuer,
  2. Andreas Okkel,
  3. Lukas Schwach,
  4. Laura Wagner,
  5. Anja Selig and
  6. Aram Prokop
  • Full Research Paper
  • Published 17 Jul 2014

Beilstein J. Org. Chem. 2014, 10, 1630–1637, doi:10.3762/bjoc.10.169

Theoretical study of the adsorption of benzene on coinage metals

  1. Werner Reckien,
  2. Melanie Eggers and
  3. Thomas Bredow
  • Full Research Paper
  • Published 04 Aug 2014

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  • Supp. Info

Beilstein J. Org. Chem. 2014, 10, 1775–1784, doi:10.3762/bjoc.10.185

Macrocyclic bis(ureas) as ligands for anion complexation

  1. Claudia Kretschmer,
  2. Gertrud Dittmann and
  3. Johannes Beck
  • Full Research Paper
  • Published 12 Aug 2014

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  • Supp. Info

Beilstein J. Org. Chem. 2014, 10, 1834–1839, doi:10.3762/bjoc.10.193

A new charge-tagged proline-based organocatalyst for mechanistic studies using electrospray mass spectrometry

  1. J. Alexander Willms,
  2. Rita Beel,
  3. Martin L. Schmidt,
  4. Christian Mundt and
  5. Marianne Engeser
  • Full Research Paper
  • Published 28 Aug 2014

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Beilstein J. Org. Chem. 2014, 10, 2027–2037, doi:10.3762/bjoc.10.211

  • Full Research Paper
  • Published 01 Sep 2014

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  • Supp. Info

Beilstein J. Org. Chem. 2014, 10, 2055–2064, doi:10.3762/bjoc.10.213

  • Full Research Paper
  • Published 23 Sep 2014

  • PDF

Beilstein J. Org. Chem. 2014, 10, 2243–2254, doi:10.3762/bjoc.10.233

  • Full Research Paper
  • Published 26 Nov 2014

  • PDF

Beilstein J. Org. Chem. 2014, 10, 2774–2782, doi:10.3762/bjoc.10.294

Mono- and multilayers of molecular spoked carbazole wheels on graphite

  1. Stefan-S. Jester,
  2. A. Vikas Aggarwal,
  3. Daniel Kalle and
  4. Sigurd Höger
  • Full Research Paper
  • Published 27 Nov 2014

  • PDF

  • Supp. Info

Beilstein J. Org. Chem. 2014, 10, 2783–2788, doi:10.3762/bjoc.10.295

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