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  2. 1,3-Dipolar cycloaddition - Wikipedia

    en.wikipedia.org/wiki/1,3-Dipolar_cycloaddition

    [1] [2] Hence, the reaction is sometimes referred to as the Huisgen cycloaddition (this term is often used to specifically describe the 1,3-dipolar cycloaddition between an organic azide and an alkyne to generate 1,2,3-triazole). 1,3-dipolar cycloaddition is an important route to the regio-and stereoselective synthesis of five-membered ...

  3. 1,3-dipole - Wikipedia

    en.wikipedia.org/wiki/1,3-dipole

    They are reactants in 1,3-dipolar cycloadditions. [1] [2] The dipole has at least one resonance structure with positive and negative charges having a 1,3 relationship which can generally be denoted as + a−b−c −, where a may be a carbon, oxygen or nitrogen, b may be nitrogen or oxygen, and c may be a carbon, oxygen or nitrogen. [3]

  4. Azide-alkyne Huisgen cycloaddition - Wikipedia

    en.wikipedia.org/wiki/Azide-alkyne_Huisgen_cyclo...

    [3] Thermal Huisgen 1,3-dipolar cycloaddition. In the reaction above [4] azide 2 reacts neatly with alkyne 1 to afford the product triazole as a mixture of 1,4-adduct (3a) and 1,5-adduct (3b) at 98 °C in 18 hours. The standard 1,3-cycloaddition between an azide 1,3-dipole and an alkene as dipolarophile has largely been ignored due to lack of ...

  5. Cycloaddition - Wikipedia

    en.wikipedia.org/wiki/Cycloaddition

    In this notation, a Diels-Alder reaction is a (4+2)cycloaddition and a 1,3-dipolar addition such as the first step in ozonolysis is a (3+2)cycloaddition. The IUPAC preferred notation however, with [i+j+...] takes electrons into account and not atoms. In this notation, the DA reaction and the dipolar reaction both become a [4+2]cycloaddition.

  6. Nitrone-olefin (3+2) cycloaddition - Wikipedia

    en.wikipedia.org/wiki/Nitrone-olefin_(3+2...

    The nitrone-olefin (3+2) cycloaddition reaction is the combination of a nitrone with an alkene or alkyne to generate an isoxazoline or isoxazolidine via a (3+2) cycloaddition process. [1] This reaction is a 1,3-dipolar cycloaddition , in which the nitrone acts as the 1,3-dipole , and the alkene or alkyne as the dipolarophile.

  7. Bioorthogonal chemistry - Wikipedia

    en.wikipedia.org/wiki/Bioorthogonal_chemistry

    1,3 dipolar cycloadditions have been developed as a bioorthogonal reaction using a nitrile oxide as a 1,3-dipole and a norbornene as a dipolarophile. Its primary use has been in labeling DNA and RNA in automated oligonucleotide synthesizers, [31] and polymer crosslinking in the presence of living cells. [32]

  8. Dipolar compound - Wikipedia

    en.wikipedia.org/wiki/Dipolar_compound

    In organic chemistry, a dipolar compound or simply dipole is an electrically neutral molecule carrying a positive and a negative charge in at least one canonical description. In most dipolar compounds the charges are delocalized . [ 1 ]

  9. Rolf Huisgen - Wikipedia

    en.wikipedia.org/wiki/Rolf_Huisgen

    Rolf Huisgen (German:; 13 June 1920 – 26 March 2020) was a German chemist.His importance in synthetic organic chemistry extends to the enormous influence he had in post-war chemistry departments in Germany and Austria, due to a large number of his habilitants becoming professors.