New transformation of cycloalkanone acetals by peracids α,ω-dicarboxylic acids synthesis Full article
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Open Chemistry
ISSN: 2391-5420 |
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| Output data | Year: 2005, Volume: 3, Number: 3, Pages: 417-431 Pages count : 15 DOI: 10.2478/bf02479272 | ||
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Abstract:
A new process of oxidation of cycloalkanone acetals under the action ofin situgenerated performic acid has been found. The main products of the reaction areα,ω-dicarboxylic acids obtained with the yield up to 77 % depending on the size of acetals ring. Theprocess has been explored and optimized on the example of thedodecanedioic acid synthesis (avaluable industrial product).
Cite:
Terent'ev A.
, Chodykin S.
New transformation of cycloalkanone acetals by peracids α,ω-dicarboxylic acids synthesis
Open Chemistry. 2005. V.3. N3. P.417-431. DOI: 10.2478/bf02479272 WOS OpenAlex
New transformation of cycloalkanone acetals by peracids α,ω-dicarboxylic acids synthesis
Open Chemistry. 2005. V.3. N3. P.417-431. DOI: 10.2478/bf02479272 WOS OpenAlex
Identifiers:
| Web of science: | WOS:000230619800005 |
| OpenAlex: | W2063275186 |