Масштабований синтез первинних амінів на основі реакції Петасіса

The efficient and scalable synthesis of homoallylic amines is a subject of significant interest due to the potential applications of these compounds in medicinal and synthetic chemistry. The three-component Petasis reaction is an excellent approach for obtaining these compounds. Based on previous st...

Повний опис

Збережено в:
Бібліографічні деталі
Дата:2025
Автори: Ryabukhin, Serhiy V., Herasymchuk, Maksym V.
Формат: Стаття
Мова:English
Опубліковано: National University of Pharmacy 2025
Теми:
Онлайн доступ:https://ophcj.nuph.edu.ua/article/view/324183
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Назва журналу:Journal of Organic and Pharmaceutical Chemistry

Репозитарії

Journal of Organic and Pharmaceutical Chemistry
Опис
Резюме:The efficient and scalable synthesis of homoallylic amines is a subject of significant interest due to the potential applications of these compounds in medicinal and synthetic chemistry. The three-component Petasis reaction is an excellent approach for obtaining these compounds. Based on previous studies, this work explores the α-aminoallylation of ketones and aldehydes using allylboronic acid pinacol ester. Compared to classical methods, the protocol developed reduces the excess of reagents, increasing the environmental friendliness of the process, while maintaining high yields. A wide range of substrates, including various aliphatic, cyclic, and heterocyclic ketones, was studied to identify factors affecting the reactivity. The method was also successfully applied to aldehydes, producing amine-containing building blocks on a large scale. Various work-up procedures were optimized for efficient isolation of the homoallylamines synthesized without the need for chromatographic purification.