Synthesis of Dimethyl (Z)-((3-oxoindolin-2-ylidene) (aryl)methyl)phosphonates Through Tandem Cadogan and Arbuzov Reactions

A novel method employing a tandem Cadogan and Arbuzov reaction sequence has been developed, providing access to a series of previously unreported dimethyl (Z)-((3-oxoindolin-2-ylidene)(aryl)methyl)phosphonates. Restricted rotation of the aryl substituent, particularly in the presence of ortho substituents, gives axial chirality to these compounds.

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Journal
Molbank
Published
2025-05-05
DOI
https://doi.org/10.3390/m2002
Primary Topic
Synthesis and Reactivity of Heterocycles
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis of Dimethyl (Z)-((3-oxoindolin-2-ylidene) (aryl)methyl)phosphonates Through Tandem Cadogan and Arbuzov Reactions

Daniil D. Ganusenko, Дмитрий А. Аксенов, Nicolai A. Aksenov, А. В. Аксенов et al.
Molbank
Synthesis and Reactivity of Heterocycles
article

Synthesis of Dimethyl (Z)-((3-oxoindolin-2-ylidene) (aryl)methyl)phosphonates Through Tandem Cadogan and Arbuzov Reactions

Daniil D. Ganusenko, Дмитрий А. Аксенов, Nicolai A. Aksenov, А. В. Аксенов, Alexander E. Kurlikov, Alexander P. Barbolin, Polina S. Karaseva
article en

Abstract

A novel method employing a tandem Cadogan and Arbuzov reaction sequence has been developed, providing access to a series of previously unreported dimethyl (Z)-((3-oxoindolin-2-ylidene)(aryl)methyl)phosphonates. Restricted rotation of the aryl substituent, particularly in the presence of ortho substituents, gives axial chirality to these compounds.

MolbankVol. 2025(2)
North-Caucasus Federal University (RU)
Russian Science Foundation
Openalex Percentile: Top 93%
Synthesis and Reactivity of Heterocycles
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