Bradsher cycloaddition
Named reactionCycloaddition
The Bradsher cycloaddition reaction, also known as the Bradsher cyclization reaction is a form of the Diels–Alder reaction which involves the [4+2] addition of a common dienophile with a cationic aromatic azadiene such as acridizinium or isoquinolinium.
More cycloaddition reactions
- Azide-alkyne Huisgen cycloaddition
- Intramolecular Diels–Alder cycloaddition
- Diels–Alder cycloaddition: cyclopentadiene + maleic anhydride → endo-norbornene-2,3-dicarboxylic anhydride
- 7α-Acetoxy-(1Hβ, 6Hβ)-bicyclo[4.4.1]undeca-2,4,8-triene via chromium-mediated higher order cycloaddition
- An improved preparation of 3-bromo-2H-pyran-2-one: an ambiphilic diene for Diels-Alder cycloadditions
- Copper(I)-catalyzed photocycloaddition: 3,3-dimethyl-cis-bicyclo[3.2.0]heptan-2-one