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Reaction Products of β-Aminopropioamidoximes Nitrobenzenesulfochlorination: Linear and Rearranged to Spiropyrazolinium Salts with Antidiabetic Activity.
Kayukova L, Vologzhanina A, Dorovatovskii P, Baitursynova G, Yergaliyeva E, Kurmangaliyeva A, Shulgau Z, Adekenov S, Shaimerdenova Z, Akatan K. Kayukova L, et al. Among authors: baitursynova g. Molecules. 2022 Mar 28;27(7):2181. doi: 10.3390/molecules27072181. Molecules. 2022. PMID: 35408580 Free PMC article.
Crystal structure and antidiabetic activity of 2-aminospiropyrazolinium tosylates and the product of O-tosylation of β-(benzimidazol-1-yl)propioamidoxime.
Kayukova LA, Vologzhanina AV, Yergaliyeva EM, Baitursynova GP, Shulgau ZT, Sergazy S. Kayukova LA, et al. Among authors: baitursynova gp. Acta Crystallogr C Struct Chem. 2022 Oct 1;78(Pt 10):542-551. doi: 10.1107/S2053229622008464. Epub 2022 Sep 11. Acta Crystallogr C Struct Chem. 2022. PMID: 36196787
Boulton-Katritzky Rearrangement of 5-Substituted Phenyl-3-[2-(morpholin-1-yl)ethyl]-1,2,4-oxadiazoles as a Synthetic Path to Spiropyrazoline Benzoates and Chloride with Antitubercular Properties.
Kayukova L, Vologzhanina A, Praliyev K, Dyusembaeva G, Baitursynova G, Uzakova A, Bismilda V, Chingissova L, Akatan K. Kayukova L, et al. Among authors: baitursynova g. Molecules. 2021 Feb 12;26(4):967. doi: 10.3390/molecules26040967. Molecules. 2021. PMID: 33673047 Free PMC article.