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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2020 Volume 30, Issue 3, Pages 372–373 (Mi mendc1201)

This article is cited in 2 papers

Communications

Taking diazo transfer to water: α-diazo carbonyl compounds from in situ generated mesyl azide

R. Shevalev, P. A. Zhmurov, D. V. Dar'in, M. Yu. Krasavin

Institute of Chemistry, St. Petersburg State University, St. Petersburg, Russian Federation

Abstract: Mesyl azide generated in situ in aqueous medium converted a range of active methylene substrates into the corresponding diazo compounds in good yields and high purity with no need for chromatographic purification. The products thus obtained are suitable for the subsequent RhII-catalyzed O–H insertions with no need for chromatography in the interim.

Keywords: diazo transfer, sulfonyl azides, in situ generation, mesyl azide, active methylene compounds, aqueous medium.

Language: English

DOI: 10.1016/j.mencom.2020.05.037



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