Synthesis of 2,2-diallyl-substituted aziridine derivatives based on reductive diallylation of amino acids

Synthesis of 2,2-diallyl-substituted aziridine derivatives based on reductive diallylation of amino acids Full article

Journal

Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285

Output data

Year: 2026, Volume: 75, Number: 3, Pages: 939-944 Pages count : 6 DOI: 10.1007/s11172-026-4948-8

Authors

Starykh S.A. ¹ , Gulyaeva E.A. ¹ , Baranin S.V. ¹ , Bubnov Yu.N. ^2,1

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation
2	A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 1 Build., 28 ul. Vavilova, 119334, Moscow, Russian Federation

Intramolecular cyclization of β-amino alcohols, obtained by reductive diallylation of racemic mixtures of amino acids, furnished the corresponding 2,2-diallyl-substituted aziridine derivatives. The latter can be efficient starting compounds for the preparation of spiro compounds containing aziridine and cyclopentene fragments.

Starykh S.A. , Gulyaeva E.A. , Baranin S.V. , Bubnov Y.N.
Synthesis of 2,2-diallyl-substituted aziridine derivatives based on reductive diallylation of amino acids
Russian Chemical Bulletin. 2026. V.75. N3. P.939-944. DOI: 10.1007/s11172-026-4948-8 WOS Scopus OpenAlex

Старых С.А. , Гуляева Е.А. , Баранин С.В. , Бубнов Ю.Н.
Синтез 2,2-диаллилзамещенных производных азиридина на основе восстановительного диаллилирования аминокислот
Известия Академии наук. Серия химическая. 2026. Т.75. №3. С.939-944.

Submitted:	Jul 26, 2025
Published online:	Apr 25, 2026

≡ Web of science:	WOS:001748883400005
≡ Scopus:	2-s2.0-105037541672
≡ OpenAlex:	W7155622309