reviewAngewandte Chemie International EditionJan 9, 2007Closed access

1,3‐Dipolar Cycloadditions of Azides and Alkynes: A Universal Ligation Tool in Polymer and Materials Science

Fraunhofer Institute for Applied Polymer Research

PubMed
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Abstract

In 2001, Sharpless and co-workers introduced "click" chemistry, a new approach in organic synthesis that involves a handful of almost perfect chemical reactions. Among these carefully selected reactions, Huisgen 1,3-dipolar cycloadditions were shown to be the most effective and versatile and thus became the prime example of click chemistry. Hence, these long-neglected reactions were suddenly re-established in organic synthesis and, in particular, have gained popularity in materials science. The number of publications dealing with click chemistry has grown exponentially over the last two years. The Minireview discusses whether click chemistry is a miracle tool or an ephemeral trend.

Citation impact

1,494
total citations
FWCI
103.74
Percentile
100%
References
105
Citations per year

Authors

1

Topics & keywords

Keywords
  • Click chemistry
  • Chemistry
  • Computational chemistry
  • Computer science
  • Polymer science
  • Organic chemistry
  • Nanotechnology
  • Materials science
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