Swern oxidation
Darzens reaction
hydroxyaldehyde
Fischer indole synthesis
acetal
homobaldrinal
aldol reaction
oxoaldehyde
Eschenmoser fragmentation
Étard reaction
Pinnick oxidation
Grignard reaction
Kornblum-DeLaMare rearrangement
Wolff rearrangement
salicylaldehyde
flavonal
hydroformylation
Cannizzaro reaction
haloaldehyde
methiodide
isoneral
Wohl-Ziegler reaction
Norrish reaction
semicarbazone
ethiodide
transaldimination
alkanal
isovaleraldehyde
acetaldehyde
alcohol dehydrogenase
hydrocarboxylation
amyl alcohol
carboxylated
baldrinal
trialdehyde
Reformatsky reaction
arylaldehyde
Suzuki reaction
oxymethylene
alkenal
isocitral
Wacker process
isoaldehyde
Horner-Wadsworth-Emmons reaction
benzyl alcohol
aldolization
carbaldehyde
isoamyl
aromatize
Darzens halogenation
acetalize
aldoxime
Meerwein-Ponndorf-Verley reduction
epoxidate
protocatechualdehyde
ammoxidation
hydroperoxidation
metapyrocatechase
hydroacylation
redox
oxidation-reduction
dinitrophenylhydrazine
oxidoreduction
naphthaldehyde
oxopentanoate
crotanaldehyde
isobutanol
monoaldehyde
hydramide
dialdehyde
semioxamazone
isovanillin
methylglyoxal
Prevost reaction
arylsulfonylation
thial
aldol
thioaldehyde
ethyl mercaptan
aldoketoreductase
ketoaldehyde
isobutyraldehyde
cycloaromatization
syringaldehyde
hydroxybenzaldehyde
acrylaldehyde
ester
formyl
stearaldehyde
chloroacetaldehyde
dipolarophile
sandalore
dialdehydic
-al
aldehyde oxidase
alkynylaldehyde
vincinal
transetherification
Wittig reaction

English words for 'A chemical reaction whereby a primary or secondary alcohol is oxidized to an aldehyde or ketone using oxalyl chloride, dimethyl sulfoxide (DMSO) and an organic base such as triethylamine.'

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