Synlett
DOI: 10.1055/a-2689-2231
Letter

Synthesis of Azetidine Nitrones by Double Methylene Incorporation into Nitrile Oxides Using Diazomethane

Ryo Iwamoto
Division of Material Chemistry, Graduate School of Natural Science and Technology, Kanazawa University, Kakuma, Kanazawa, Ishikawa 920-1192, Japan (Ringgold ID: RIN12858)
,
Takuya Suga
Division of Material Chemistry, Graduate School of Natural Science and Technology, Kanazawa University, Kakuma, Kanazawa, Ishikawa 920-1192, Japan (Ringgold ID: RIN12858)
,
Takahiro Soeta
Division of Material Chemistry, Graduate School of Natural Science and Technology, Kanazawa University, Kakuma, Kanazawa, Ishikawa 920-1192, Japan (Ringgold ID: RIN12858)
,
Yutaka Ukaji
Division of Material Chemistry, Graduate School of Natural Science and Technology, Kanazawa University, Kakuma, Kanazawa, Ishikawa 920-1192, Japan (Ringgold ID: RIN12858)
› Institutsangaben

This research was partly supported by a Grant-in-Aid for Scientific Research (C) (24K08426) from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan.


Preview

Abstract

A novel method for preparing 4-membered azetidine nitrones, starting from isolable nitrile oxides, has been developed. The reaction of diazomethane with the bulky nitrile oxides proceeds via double nucleophilic incorporation of the methylene moiety to produce 4-membered cyclic nitrones in yields up to 74%. A reaction pathway involving the formation of a strained azirine N-oxide intermediate is discussed.

Supplementary Material



Publikationsverlauf

Eingereicht: 20. Juli 2025

Angenommen nach Revision: 24. August 2025

Accepted Manuscript online:
24. August 2025

Artikel online veröffentlicht:
18. September 2025

© 2025. Thieme. All rights reserved.

Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany

 
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