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5-arylethynyl-1,4-naphthoquinones

Journal Article · · Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States)
OSTI ID:7222515
; ; ;
The introduction of the acetylenic substituent in position 5 of 1,4-naphthoquinones is carried out by condensing the iodoquinone with the cuprous derivative of the substituted acetylene. The starting iodide was obtained by diazotization of 5-amino-1,4-dihydroxynaphthalene, which was oxidized by FeCl/sub 3/ without separation.
Research Organization:
Institute of Chemical Kinetics and Combustion, Siberian Branch, Academy of Sciences, Novosibirsk
OSTI ID:
7222515
Journal Information:
Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States), Journal Name: Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States) Vol. 33:11, PT. 2; ISSN BACCA
Country of Publication:
United States
Language:
English

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Related Subjects

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
400201* -- Chemical & Physicochemical Properties
ACETYLATION
ACYLATION
ALKYNES
AROMATICS
AZO COMPOUNDS
CATALYTIC EFFECTS
CERIUM COMPLEXES
CHALCOGENIDES
CHEMICAL REACTION YIELD
CHEMICAL REACTIONS
CHLORIDES
CHLORINE COMPOUNDS
CHROMIUM COMPOUNDS
CHROMIUM OXIDES
COMPLEXES
CONDENSED AROMATICS
COPPER COMPLEXES
DEHYDROCYCLIZATION
HALIDES
HALOGEN COMPOUNDS
HALOGENATED AROMATIC HYDROCARBONS
HALOGENATION
HYDROCARBONS
IODINATED AROMATIC HYDROCARBONS
IODINATION
IRON CHLORIDES
IRON COMPOUNDS
NAPHTHALENE
ORGANIC COMPOUNDS
ORGANIC HALOGEN COMPOUNDS
ORGANIC IODINE COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANIC OXYGEN COMPOUNDS
OXIDATION
OXIDES
OXYGEN COMPOUNDS
QUINONES
RARE EARTH COMPLEXES
SYNTHESIS
TRANSITION ELEMENT COMPLEXES
TRANSITION ELEMENT COMPOUNDS
YIELDS