1989
DOI: 10.1002/chin.198952151
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ChemInform Abstract: Synthesis, Properties and Application of Ethers Derived from 4‐Hydroxymethyl‐1,3‐dioxolane.

Abstract: The title compounds (III) are tested for their inhibitory activity towards the sulfate‐reducing bacteria Desulfovibrio desulfuricans.

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“…The reaction of vicinal diols with carbonyl addends is an accessible method of synthesis of five-membered heterocycles with vicinal dioxogroups -1,3-dioxolanes [1][2][3]. The cyclic acetals of 1,3-dioxolane series are applied as plasticizers [4], modifiers [5], solvents of cellulose esters [6], metal corrosion inhibitors [7] and substances intensifying oil extraction [8] etc. In addition, they are of the utmost interest as perspective monomers for polymerization processes [9]; intermediate compounds in the synthesis of biologically active and pharmaceutical preparations [10].…”
mentioning
confidence: 99%
“…The reaction of vicinal diols with carbonyl addends is an accessible method of synthesis of five-membered heterocycles with vicinal dioxogroups -1,3-dioxolanes [1][2][3]. The cyclic acetals of 1,3-dioxolane series are applied as plasticizers [4], modifiers [5], solvents of cellulose esters [6], metal corrosion inhibitors [7] and substances intensifying oil extraction [8] etc. In addition, they are of the utmost interest as perspective monomers for polymerization processes [9]; intermediate compounds in the synthesis of biologically active and pharmaceutical preparations [10].…”
mentioning
confidence: 99%