Claisen rearrangement
epoxidate
alkoxycyclization
acetylenic
ruthenation
heteroalkene
hydroxycyclization
quaiacol
hexadiene
gem-disubstituent effect
oxocarbazate
monocarbonylation
carbonylic
bicycloheptadiene
Schmidt reaction
carbonylation
Stetter reaction
adamantanone
di-pimethane rearrangement
pentene
Mannich reaction
diacetylenic
oxo-
hydroazafullerene
polyunsaturated
hyperfullerene
propargylamide
carbamylation
pentyne
ethenium
thiazolidinone
etabonic acid
cycloheptatrienone
Claisen condensation
ketocarbene
dihaloelimination
oxoindolizidine
cyclopropenone
organoantimony
carbyne
aldotrionic acid
carbonyl
oligoene
keto
ketoalkene
carbamoylate
-oxy
hexene
carbon-carbon bond
propargylic
carbonimidic
ethynium
thiopyrylium
omega-3 fatty acid
aldotetronic acid
oxocarboxylate
oxopiperazine
iminobiotin
organocarbon
terminal acetylene
aldopentonic acid
aldohexonic acid
decatetraene
cyclooctyne
omega-3
quinuclidinone
diazaphenanthrene
activated charcoal
naphthalenone
carbonylatable
diheterabenzene
pentacarbonyl
oxoderivative
ketotetrose
photohydration
stannyne
tetracarbon
dicarbonylation
hexadecene
hydroheterofullerene
Arndt-Eistert synthesis
organotungsten
tungstacyclopentane
hydromethylation
azaphenalene
indotricarbocyanine
protodeauration
tetracarbide
cation-π
hypercarbonylation
ketocarbenoid
prop-
azapurine
organometallic
lampblack
quinonoid
acetylene
bridged carbocation

English words for 'A powerful carbon–carbon bond-forming chemical reaction, in which the heating of an allyl vinyl ether initiates a [3,3]-sigmatropic rearrangement to give a γ,δ-unsaturated carbonyl.'

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