16244-26-1Relevant articles and documents
Synthesis and photochemistry of photochromic fluorescing indol-2-ylfulgimides
Liang,Dvornikov,Rentzepis
, p. 2477 - 2482 (2007/10/03)
A series of N-substituted, thermally stable, photochromic fluorescing indol-2-ylfulgimides were synthesized, with high yields, from the corresponding fulgides by Lewis acid and hexamethyldisilazane promoted one-pot reaction. The quantum efficiencies of the photoinduced coloration and bleaching processes, in polar and nonpolar solvents, were determined. The fluorescence quantum yields of the colored form as well as the thermal stability and fatigue resistances of the synthesized fulgimides were also determined.
Addition of Dimethyl Acetylenedicarboxylate to 1,2,3-Trisubstituted Indoles having no Hydrogen on the Carbon Atom attached to C-2.
Letcher, Roy M.,Wai, John S. M.
, p. 514 - 536 (2007/10/02)
Addition of dimethyl acetylenedicarboxylate to seven 1,2,3-trisubstituted indoles having no hydrogen on the carbon atom attached to C-2, has yielded fourteen adducts which are mainly fused γ-lactones, but which include a new phenanthridine-dione, a novel spiro-dihydroindole, and a carbazole formed by the loss of methane.All structures were elucidated by spectroscopy.
