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.

Original languageEnglish
Pages (from-to)372-373
Number of pages2
JournalMendeleev Communications
Volume30
Issue number3
Early online date6 Jun 2020
DOIs
StatePublished - 2020

    Scopus subject areas

  • Chemistry(all)

    Research areas

  • active methylene compounds, aqueous medium, diazo transfer, in situ generation, mesyl azide, sulfonyl azides, KETONES

ID: 59750682