1–3 of 3

  1. Azide-alkyne Huisgen cycloadditionCycloaddition The azide-alkyne Huisgen cycloaddition is a 1,3-dipolar cycloaddition between an azide and a terminal or internal alkyne to give a 1,2,3-triazole. Named reaction · Wikipedia
  2. Bradsher cycloadditionCycloaddition 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. Named reaction · Wikipedia
  3. Intramolecular Diels–Alder cycloadditionCycloaddition In organic chemistry, an intramolecular Diels-Alder cycloaddition is a Diels–Alder reaction in which the diene and the dienophile are both part of the same molecule. Named reaction · Wikipedia