Ullmann condensation
Zincke nitration
arylpropyne
Eschenmoser fragmentation
arylalkylidene
diarylation
arylacetaldehyde
arylpyrrolidine
Sandmeyer reaction
alkylarylamine
acyloxylation
aryloxypyrimidine
arylacetamide
lysophosphatidylcholine
fluorosilane
arylpyrrole
diarylamide
lysophosphatide
ammonium
argininal
arylcarboxylic
diarylamine
arylacetylene
arylalkyne
aryldiacetylene
dimethylarginine
lysophosphatidylserine
lysophosphatidylethanolamine
biraryl
arylamination
benzoylarginine
hydrophenoxylation
carbinamine
acylphenol
Suzuki reaction
aralkyl
methylarginine
carboamination
arylnaphthalene
organophosphorus
hydroarylation
acetylide
hydroacylation
arylating
arylazole
cyanamide
hydroxyaryl
diaryl
arylpyridine
diarylmethylene
phenylnitrone
diacylamine
lysophosphoglyceride
isovaleronitrile
arylimidazolide
acylpyridine
arylpyrazole
arylidene
acridinyl
cyanoethyl
biaryl
cyanophosphorylation
phenylpyridine
arylthioacetamide
nitrosamine
epoxidate
aroylation
arytenoidopexy
arylazirine
lysophosphatidic
nitrosation
organometallic compound
oxyarylation
aminooxygenation
arylalkylamine
metalloaryl
arylpiperidine
arylamine
arylhydrazine
arginyl
acyloxymethyl
bisarylated
arylcopper
diarylated
aryltetracene
arylphosphine
acetamidation
radicofunctional
acetylpyridine
diaminoguanidine
acylhydroxylamine
iodolysis
dearylation
Baeyer-Villiger oxidation
dihydroxyacetophenone
dinitroaniline
nitropyridine
arylmethyl
aminoarylation
alkenylacyl

English words for 'The copper-promoted conversion of aryl halides to aryl ethers, aryl thioethers, aryl nitriles, and aryl amines. These reactions are examples of cross-coupling reactions.[1]'

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