KnowraElectrocyclic reactionLinked fromLinked fromThe 11 pages that link to Electrocyclic reaction, each with the reason it gives.All 11Broader topic 5Related 5Compared with 1Frontier molecular orbital theoryBroader topic: Frontier orbital phases predict its conrotatory or disrotatory mode.ErgosterolRelated: The ultraviolet step in vitamin D₂ formation is a photochemical ring-opening reaction.Woodward–Hoffmann rulesBroader topic: Electrocyclic reactions provide the clearest cases of orbital-symmetry control over stereochemistry.Concerted reactionBroader topic: Its terminal bond forms or breaks through coordinated shifts in the conjugated pi system.CycloadditionCompared with: It shares orbital-symmetry principles with cycloaddition but changes a different number of bonds.Pericyclic reactionBroader topic: Its conrotatory or disrotatory motion is a direct consequence of pericyclic orbital symmetry.IsomerizationRelated: Electrocyclic ring opening and closure can interconvert constitutional isomers.Stereospecific reactionRelated: Conrotatory or disrotatory motion maps reactant stereochemistry onto product stereochemistry.Alicyclic compoundRelated: Electrocyclic reactions can create or open alicyclic rings with stereochemical control.CyclopropeneRelated: Cyclopropene can undergo ring opening through a thermally allowed electrocyclic pathway.Forbidden mechanismBroader topic: Its allowed conrotatory or disrotatory motion depends on orbital symmetry and conditions.