Cycloaddition Reactions of Azides Including Bioconjugation

  • Bräse S
  • Friedrich A
  • Gartner M
  • et al.
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Abstract

A review. Org. azides R-N3, albeit being energy-rich and very reactive, are useful intermediates in org. synthesis. The cycloaddn. reaction of azides with double and triple bonds to yield heterocyclic structures - albeit being discovered many centuries ago - has evolved into a powerful tool in org. synthesis, material sciences and life sciences, and are thus covered in this review. In particular, the recent development of catalytic and therefore mild reaction conditions has led to an enormous increase of systematic investigation and novel applications. [on SciFinder(R)]

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Bräse, S., Friedrich, A., Gartner, M., & Schröder, T. (2008). Cycloaddition Reactions of Azides Including Bioconjugation. In Synthesis of Heterocycles via Cycloadditions I (pp. 45–115). Springer Berlin Heidelberg. https://doi.org/10.1007/7081_2007_104

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