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

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 <i>N</i>-heterocycles (piperidine, morpholine,...

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Bibliographic Details
Main Authors: Lyudmila Kayukova, Anna Vologzhanina, Pavel Dorovatovskii, Gulnur Baitursynova, Elmira Yergaliyeva, Ayazhan Kurmangaliyeva, Zarina Shulgau, Sergazy Adekenov, Zhanar Shaimerdenova, Kydymolla Akatan
Format: Article
Language:English
Published: MDPI AG 2022-03-01
Series:Molecules
Subjects:
β-aminopropioamidoximes
nitrobezenesulfochlorination
spiropyrazolinium salts
X-ray diffraction
Online Access:https://www.mdpi.com/1420-3049/27/7/2181

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https://www.mdpi.com/1420-3049/27/7/2181

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