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Mendeleev Communications, 1998, Volume 8, Issue 6, Pages 245–246
DOI: https://doi.org/10.1070/MC1998v008n06ABEH000971
(Mi mendc4751)
 

This article is cited in 3 scientific papers (total in 3 papers)

Synthesis of difluorodithiopyruvic acid derivatives

Yu. G. Shermolovich, V. M. Timoshenko, V. V. Listvan, L. N. Markovsky

Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev, Ukraine
Full-text PDF (126 kB) Citations (3)
Abstract: The reaction of cadmium sulfide with 1,1-dichloro-3,3-difluoro-2-oxo-1-propylthiopropane yields difluorodithiopyruvic propionate. This reacts with morpholine to give difluorodithiopyruvic morpholide; it also undergoes a cycloaddition reaction to the carbon–sulfur double bond with dimethylbutadiene to form 2-difluoroacetyl-4,5-dimethyl-2-propylthio-3H,6H-thiopyran.
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Document Type: Article
Language: English


Citation: Yu. G. Shermolovich, V. M. Timoshenko, V. V. Listvan, L. N. Markovsky, “Synthesis of difluorodithiopyruvic acid derivatives”, Mendeleev Commun., 8:6 (1998), 245–246
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  • This publication is cited in the following 3 articles:
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