Up-Scale Pseudotelescopic Photoinduced Arndt-Eistert α-Amino Acid Homologation in a Flow Reactor Cascade

We present an efficient, pseudotelescopic synthesis of β-amino acids via the Arndt-Eistert homologation of α-amino acids using a flow reactor cascade. Our system utilizes flow generation of diazomethane, diazoketone preparation, and subsequent photoflow Wolff rearrangement without intermediate isolation. This innovative method enhances safety, improves scalability, and allows access to substrates previously unavailable in thermal/catalytic Wolff rearrangement. Notably, the reaction conditions are mild, which lead to high yields and excellent purity, thereby expanding the synthetic utility of the Wolff rearrangement. This work unveils a versatile and scalable approach to β-amino acid synthesis, opening new synthetic and medicinal chemistry avenues.

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Publication Details

Journal
Organic Process Research & Development
Published
2025-05-30
DOI
https://doi.org/10.1021/acs.oprd.5c00061
Citations
2
Primary Topic
Innovative Microfluidic and Catalytic Techniques Innovation
Type
article
Field-Weighted Citation Impact
1.35

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article

Up-Scale Pseudotelescopic Photoinduced Arndt-Eistert α-Amino Acid Homologation in a Flow Reactor Cascade

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Innovative Microfluidic and Catalytic Techniques Innovation
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article

Up-Scale Pseudotelescopic Photoinduced Arndt-Eistert α-Amino Acid Homologation in a Flow Reactor Cascade

Hanna Yakovleva, Sergey V. Ryabukhin, Alexander B. Rozhenko, Dmitriy M. Volochnyuk, Olesia B. Volovenko, Ivan A. Stadniy, Viacheslav Pendiukh, Olexandr Pashenko
article en
2 citations

Abstract

We present an efficient, pseudotelescopic synthesis of β-amino acids via the Arndt-Eistert homologation of α-amino acids using a flow reactor cascade. Our system utilizes flow generation of diazomethane, diazoketone preparation, and subsequent photoflow Wolff rearrangement without intermediate isolation. This innovative method enhances safety, improves scalability, and allows access to substrates previously unavailable in thermal/catalytic Wolff rearrangement. Notably, the reaction conditions are mild, which lead to high yields and excellent purity, thereby expanding the synthetic utility of the Wolff rearrangement. This work unveils a versatile and scalable approach to β-amino acid synthesis, opening new synthetic and medicinal chemistry avenues.

Organic Process Research & DevelopmentVol. 29(6)
National Academy of Sciences of Ukraine (UA), Taras Shevchenko National University of Kyiv (UA), Institute of Organic Chemistry (UA), Enamine (Ukraine) (UA)
National Research Foundation of Ukraine
Clean water and sanitation
Openalex Percentile: Top 20%
Innovative Microfluidic and Catalytic Techniques Innovation
1.35
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Up-Scale Pseudotelescopic Photoinduced Arndt-Eistert α-Amino Acid Homologation in a Flow Reactor Cascade — Hanna Yakovleva, Sergey V. Ryabukhin, et al. · Organic Process Research & Development (2025) | TGRS Research Map | TGRS