Acetals in amidoalkylation of phosphonous carboxylic acids

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.

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Publication Details

Journal
Mendeleev Communications
Published
2025-01-01
DOI
https://doi.org/10.71267/mencom.7650
Primary Topic
Organophosphorus compounds synthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Acetals in amidoalkylation of phosphonous carboxylic acids

Sergey V. Simonov, Alexey V. Borodachev, S. R. Golovash, М. В. Дмитриев et al.
Mendeleev Communications
Organophosphorus compounds synthesis
article

Acetals in amidoalkylation of phosphonous carboxylic acids

Sergey V. Simonov, Alexey V. Borodachev, S. R. Golovash, М. В. Дмитриев, В. В. Рагулин, Dmitry E Ivanov
article en

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.

Mendeleev CommunicationsVol. 35(3)
Osipyan Institute of Solid State Physics RAS (RU), Institute of Physiologically Active Compounds (RU)
Russian Science Foundation
Openalex Percentile: Top 95%
Organophosphorus compounds synthesis
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