Mild dealkylative N-nitrosation of N,N-dialkylaniline derivatives for convenient preparation of photo-triggered and photo-calibrated NO donors

  • Shaobing Qiu
  • , Chunlei Guo
  • , Mingkang Wang
  • , Zhenglong Sun
  • , Hui Li
  • , Xuhong Qian*
  • , Youjun Yang
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

N-Nitroso push-pull dyes are unique NO donors, whose NO release is triggered by light and accompanied by a concomitant fluorescence turn-on. Their synthesis involves nitrosation of the corresponding secondary amines, which, however, are not readily available. In this manuscript, we developed a mild, convenient and high-yielding preparation of N-nitroso aryl amines via dealkylative N-nitrosation of tertiary amines. This method is readily employed for the preparation of N-nitrosated rhodamine and coumarin dyes, whose potential as novel NO donors were showcased in cultured cell lines.

Original languageEnglish
Pages (from-to)3206-3209
Number of pages4
JournalOrganic Chemistry Frontiers
Volume5
Issue number22
DOIs
StatePublished - 21 Nov 2018
Externally publishedYes

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