1152844-99-9Relevant academic research and scientific papers
Direct and facile synthesis of acyl azides from carboxylic acids using the trichloroisocyanuric acid-triphenylphosphine system
Akhlaghinia, Batool,Rouhi-Saadabad, Hamed
, p. 181 - 185 (2013)
A mild, efficient, and practical method for the one-step synthesis of acyl azides from carboxylic acids using a safe and inexpensive mixed reagent, trichloroisocyanuric acid-triphenylphosphine, is described.
Visible light sensitization of benzoyl azides: Cascade cyclization toward oxindoles: Via a non-nitrene pathway
Bagal, Dattatraya B.,Park, Sung-Woo,Song, Hyun-Ji,Chang, Sukbok
supporting information, p. 8798 - 8801 (2017/08/09)
Visible light sensitization of benzoyl azides was examined in reaction with N-phenylmethacrylamides to afford biologically important oxindoles and spirooxindoles via a cascade cyclization under mild reaction conditions. Mechanistic studies suggested a non-nitrene pathway, where triplet benzoyl azides act as the reactive intermediate.
