Catalytic synthesis of terpenoid-derived hexahydro-2H-chromenes with analgesic activity over halloysite nanotubes
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Новосибирский институт органической химии им. Н.Н. Ворожцова
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В журнале Applied Catalysis A: General   (IF=5.006) опубликована статья  с участием сотрудников Института: к.х.н. И.В. Ильиной (снс, ЛФАВ), Н.С. Ли-Жуланова (нс, ЛНТПС), к.х.н. Д.В. Корчагиной (снс, ГЯМР), к.х.н. О.В. Ардашова (снс, ЛФАВ), д.х.н., проф. РАН К.П. Волчо (гнс, ЛФАВ) и  чл.-корр. РАН, д.х.н., проф.  Н. Ф. Салахутдинова (рук. отдела ОМХ, завлаб ЛФАВ)


Catalytic synthesis of terpenoid-derived hexahydro-2H-chromenes with analgesic activity over halloysite nanotubes

A.Yu.Sidorenko, Yu.M.Kurban, I.V.Il'ina, N.S.Li-Zhulanov, D.V.Korchagina, O.V.Ardashov, J.Wärnå, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov

Applied Catalysis A: General

Volume 618, 25 May 2021, 118144


 https://doi.org/10.1016/j.apcata.2021.118144

 2021_05_25_ACGA.jpg

Abstract

Condensation of α-pinene derived p-menta-1,8-diene-5,6-diol (diol) with decanal was studied for the first time over modified halloysite nanotubes (HNT). The yield of the desired hexahydro-2H-chromene-4,8-diol with analgesic activity was 76–80 % practically not depending on the catalyst type, while selectivity to 4S-isomer decreased, and to 4R-isomer increased with increasing acidity. The highest selectivity to 4S-diastereomer (48.1 %) on halloysite is a result of weak acidity of this catalyst. DFT optimization of the key intermediate structure shows that the nucleophile attack proceeds at the equatorial position with the 4S-diastereomer formation, which was preferred on halloysite. On strong Brønsted (Amberlyst-15) and Lewis (scandium triflate) acids the target product yield did not exceed 37 % because of dehydration. Halloysite nanocatalysts displayed a stable performance. In the case of diol reaction with a set of carbonyl compounds, the yields of hexahydro-2H-chromene-4,8-diols (up to 88.0%) and the ratio of its 4S/4R isomers (up to 21.0) were significantly higher than on other catalysts.

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