Reaction Products of β-Aminopropioamidoximes Nitrobenzenesulfochlorination: Linear and Rearranged to Spiropyrazolinium Salts with Antidiabetic Activity

Reaction Products of β-Aminopropioamidoximes Nitrobenzenesulfochlorination: Linear and Rearranged to Spiropyrazolinium Salts with Antidiabetic Activity

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Nitrobenzenesulfochlorination of β-aminopropioamidoximes leads to a set of products depending on the structure of the initial interacting substances and reaction conditions. Amidoximes, functionalized at the terminal C atom with six-membered N-heterocycles (piperidine, morpholine, thiomorpholine and...

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Bibliographic Details
Main Authors: Adekenov, S. (Author), Akatan, K. (Author), Baitursynova, G. (Author), Dorovatovskii, P. (Author), Kayukova, L. (Author), Kurmangaliyeva, A. (Author), Shaimerdenova, Z. (Author), Shulgau, Z. (Author), Vologzhanina, A. (Author), Yergaliyeva, E. (Author)
Format: Article
Language:English
Published: MDPI 2022
Subjects:
antidiabetic agent
chemistry
chloride
Chlorides
hydrogen
Hydrogen
Hypoglycemic Agents
inorganic salt
nitrobezenesulfochlorination
Salts
spiropyrazolinium salts
stereoisomerism
Stereoisomerism
X-ray diffraction
β-aminopropioamidoximes
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