1,3-Dipolar cycloaddition
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The 1,3-dipolar cycloaddition, also known as the Huisgen cycloaddition or Huisgen reaction, [1] [2] is an organic chemical reaction belonging to the larger class of cycloadditions. It is the reaction between a 1,3-dipole and a dipolarophile, most of which are substituted alkenes, to form a five-membered ring. Rolf Huisgen first saw the prospects of varying the 1,3-dipole and its high value for synthesis of 5-membered heterocycles.
[edit] Classes of 1,3-dipoles
Huisgen and others investigated a range of 1,3-dipoles and dipolarophiles. These included:
- Azides and alkynes react in the Azide alkyne Huisgen cycloaddition.
- Diazo compounds are 1,3-dipoles in the Diazoalkane 1,3-dipolar cycloaddition.
- Nitrones react with alkenes to form isoxazolidines.
- Ozonolysis begins with a 1,3-dipolar cycloaddition of ozone. This is followed by a retro-1,3-dipolar cycloaddition and then a 1,3-dipolar cycloaddition of the fragments.
- Fullerenes and nanotubes can undergo a 1,3-dipolar cycloaddition with an azomethine ylide in the Prato reaction.
[edit] References
- ^ Huisgen, Rolf (November 1963). "Kinetics and Mechanism of 1,3-Dipolar Cycloadditions" (abstract). Angewandte Chemie International Edition 2 (11): 633–645. doi:.
- ^ Huisgen, Rolf (October 1963). "1,3-Dipolar Cycloadditions. Past and Future" (abstract). Angewandte Chemie International Edition 2 (10): 565–598. doi:.
[edit] External links
- [1] Click Chemicals. A new site featuring in depth discussion, faq's and links to key papers surround 1,3 dipolar cycloadditions
