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Mendeleev Communications, 2025, Volume 35, Issue 3, Pages 266–268
DOI: https://doi.org/10.71267/mencom.7650
(Mi mendc6221)
 

Communications

Acetals in amidoalkylation of phosphonous carboxylic acids

S. R. Golovasha, D. E. Ivanova, A. V. Borodacheva, S. V. Simonovb, M. E. Dmitrieva, V. V. Ragulina

a Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Moscow Region, Russian Federation
b Yu. A. Osipyan Institute of Solid State Physics, Russian Academy of Sciences, 142432 Chernogolovka, Moscow Region, Russian Federation
References:
Abstract: The use of free phosphonous carboxylic diacids in three–component carbamate version of the Kabachnik–Fields reaction in acetyl chloride medium allows introducing acetals into the reaction sphere to result in phosphinic peptides. The employment of low-stable and functionally substituted aldehydes in the form of acetals provides phosphinic peptides that are difficult to obtain by other methods.
Keywords: acetals, phosphinic pseudopeptides, phosphonous carboxylic diacids, amidoalkylation, phospha lactone, acyliminium cation, Kabachnik–Fields reaction.
Funding agency Grant number
Russian Science Foundation 23-23-00158
Received: 15.10.2024
Accepted: 05.12.2024
Published: 31.03.2025
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (2.3 Mb)


Citation: S. R. Golovash, D. E. Ivanov, A. V. Borodachev, S. V. Simonov, M. E. Dmitriev, V. V. Ragulin, “Acetals in amidoalkylation of phosphonous carboxylic acids”, Mendeleev Commun., 35:3 (2025), 266–268
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