Synthesis of new sulfonic acid derivatives by the reaction of S-(1S,2R,3S,5R)-2-formyl-6,6-dimethylnorpinan-3-yl thioacetate with chlorine dioxide
- Autores: Subbotina S.N.1, Grebyonkina O.N.1, Gribkov P.V.1, Gerasimova D.P.2, Lodochnikova O.A.2, Gilfanov I.R.3, Nikitina L.E.4, Lezina O.M.1, Rubtsova S.A.1
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Afiliações:
- Institute of Chemistry, Federal Research Center, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences
- Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences
- Kazan National Research Technological University
- Kazan State Medical University
- Edição: Volume 60, Nº 4 (2024)
- Páginas: 468-478
- Seção: Articles
- URL: https://archivog.com/0514-7492/article/view/672164
- DOI: https://doi.org/10.31857/S0514749224040079
- EDN: https://elibrary.ru/RZBKIO
- ID: 672164
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Resumo
New polyfunctional compounds of the pinane series, 2-carboxy-3-thioacetate, 2-carboxy-3-sulfonyl chloride, and 2-carboxy-3-sulfonic acid that are promising intermediate products in organic synthesis, were synthesized for the first time by the reaction of S-(1S,2R,3S,5R)-(6,6-dimethyl-2-formylnorpinan-3-yl) thioacetate with chlorine dioxide. The major reaction pathway in nonpolar solvents involves oxidation of the aldehyde group to carboxy, whereas oxidation of the sulfur atom, followed by deacetylation, occurs in highly polar solvents. The effect of VO(acac)2 as catalyst on the reaction chemoselectivity in weakly polar diethyl ether was revealed.
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Sobre autores
S. Subbotina
Institute of Chemistry, Federal Research Center, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences
Email: lezina-om@yandex.ru
ORCID ID: 0009-0001-0512-3478
Rússia, ul. Pervomayskaya, 48, Syktyvkar, 167000
O. Grebyonkina
Institute of Chemistry, Federal Research Center, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences
Email: lezina-om@yandex.ru
ORCID ID: 0000-0002-1982-104X
Rússia, ul. Pervomayskaya, 48, Syktyvkar, 167000
P. Gribkov
Institute of Chemistry, Federal Research Center, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences
Email: lezina-om@yandex.ru
ORCID ID: 0000-0003-2923-4620
Rússia, ul. Pervomayskaya, 48, Syktyvkar, 167000
D. Gerasimova
Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences
Email: lezina-om@yandex.ru
ORCID ID: 0000-0001-9770-196X
Rússia, ul. Arbuzova, 8, Kazan, 420088
O. Lodochnikova
Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences
Email: lezina-om@yandex.ru
ORCID ID: 0000-0001-9614-5092
Rússia, ul. Arbuzova, 8, Kazan, 420088
I. Gilfanov
Kazan National Research Technological University
Email: lezina-om@yandex.ru
ORCID ID: 0000-0003-4351-3378
Rússia, ul. K. Marksa, 68, Kazan, 420015
L. Nikitina
Kazan State Medical University
Email: lezina-om@yandex.ru
ORCID ID: 0000-0003-2113-5732
Rússia, ul. Butlerova, 49, Kazan, 420012
O. Lezina
Institute of Chemistry, Federal Research Center, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences
Autor responsável pela correspondência
Email: lezina-om@yandex.ru
ORCID ID: 0000-0002-6105-5641
Rússia, ul. Pervomayskaya, 48, Syktyvkar, 167000
S. Rubtsova
Institute of Chemistry, Federal Research Center, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences
Email: lezina-om@yandex.ru
ORCID ID: 0000-0003-1224-8751
Rússia, ul. Pervomayskaya, 48, Syktyvkar, 167000
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