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Mendeleev Communications, 2025, Volume 35, Issue 5, Pages 521–523
DOI: https://doi.org/10.71267/mencom.7744
(Mi mendc7278)
 

Communications

Synthesis of 3-amino triterpenes involving the NaBH3CN/MoCl5 reduction of the oxime precursors

A. A. Shalinaa, L. R. Idrisovaa, A. V. Nemtarevab, T. I. Abdullina, V. F. Mironovb

a Kazan (Volga Region) Federal University, 420008 Kazan, Russian Federation
b A. E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, 420088 Kazan, Russian Federation
References:
Abstract: A new efficient method for the preparation of 3-amino derivatives of pentacyclic lupane and germanicane triterpenoids, valuable precursors for the rational design of physiologically active agents, is presented. The key step involves the reduction of triterpenoid 3-oximes with sodium cyanoborohydride in the presence of molybdenum(v) chloride.
Keywords: triterpenes, betulin, allobetulin, lupane type, molybdenum(v) chloride, reduction reaction, sodium cyanoborohydride, oximes, amines.
Funding agency Grant number
Ministry of Science and Higher Education of the Russian Federation FZSM-2023-0018
PRIORITY-2030
Russian Science Foundation 20-73-10105
Received: 07.02.2025
Accepted: 31.03.2025
Published: 17.07.2025
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (3.8 Mb)


Citation: A. A. Shalina, L. R. Idrisova, A. V. Nemtarev, T. I. Abdullin, V. F. Mironov, “Synthesis of 3-amino triterpenes involving the NaBH3CN/MoCl5 reduction of the oxime precursors”, Mendeleev Commun., 35:5 (2025), 521–523
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