26977-47-9Relevant articles and documents
1,4,2-Dioxazol-5-ones as Isocyanate Equivalents: Chemoselective Non-Metal-Catalyzed Carboxamidation of Indoles
Vala, Anand,Parmar, Deepa,Rayani, Rahul,Kusurkar, Rakesh,Guduru, Ramakrishna,Kaneriya, Uttam,Gondaliya, Uday,Parmar, Nirali,Soni, Jigar Y.
, (2022/02/21)
1,4,2-Dioxazol-5-ones are known to undergo decarboxylation under thermal conditions followed by Lossen s rearrangement to give isocyanates. Described herein is the in situ trapping of the isocyanates by indoles to give indole-3-carboxamides in good to exc
Synthesis of 4,6-disubstituted-2-(1H-indol-3-yl)-benzothiazoles
Zaletova, Janka,Dzurilla, Milan,Kutschy, Peter,Pazdera, Pavel,Kovacik, Vladimir,Aldoelfi, Juraj,Bekesova, Slavka
, p. 453 - 460 (2007/10/03)
A new four-step synthesis of substituted 2-(1H-indol-3-yl)benzothiazoles is described, using N3-phenyl-1H-indole-3-carbothioamides as key intermediates. The structure of the obtained products was determined by IR, 1H, 13C NMR and MS spectral methods.