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Electrosynthesis of esters of mono- and dioxoalkanoic and alkanedioic acids on the basis of nitro-substituted alkyl carboxylates and cycloalkanones Full article

Journal Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Output data Year: 2003, Volume: 52, Number: 3, Pages: 728-733 Pages count : 6 DOI: 10.1023/a:1023935629115
Authors Ogibin Yu.N. 1 , Ilovaiskii A.I. 1 , Merkulova V.M. 1 , Nikishin G.I. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation

Abstract: A one-pot electrochemical method for the synthesis of methyl monooxoalkanoates with the carbonyl group in position 4, methyl dioxoalkanoates with the oxo groups in positions 4,7-, 6,9-, 7,10-, and 12,15, and methyl 4-oxoalkanedioates was developed. This method is based on amperostatic electrolysis in an undivided cell of the salts of esters of nitroalkaniic acids and their adducts with CH2=CHX (X = Ac, CO2Me).
Cite: Ogibin Y.N. , Ilovaiskii A.I. , Merkulova V.M. , Nikishin G.I.
Electrosynthesis of esters of mono- and dioxoalkanoic and alkanedioic acids on the basis of nitro-substituted alkyl carboxylates and cycloalkanones
Russian Chemical Bulletin. 2003. V.52. N3. P.728-733. DOI: 10.1023/a:1023935629115 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000183739500032
Scopus: 2-s2.0-0038323226
OpenAlex: W2949702678
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OpenAlex 3
Scopus 2
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