94193-98-3Relevant academic research and scientific papers
Diels-Alder Reactivity of Pyranoindol-3-ones, Stable Analogues of Indole-2,3-quinodimethanes
Moody, Christopher J.
, p. 2505 - 2508 (2007/10/02)
The Pyranoindol-3-ones (13a,b), stable synthetic analogues of indole-2,3-quinodimethanes, undergo Diels-Alder reactions with acetylenes to give, with concomitant loss of carbon dioxide, carbazoles.Thus, reaction with dimethyl acetylenedicarboxylate
Diels-Alder Reactivity of Pyranoindol-3-ones, Stable, Synthetic Equivalents of Indole-2,3-quinodimethanes
Moody, Christopher J.
, p. 925 - 926 (2007/10/02)
Pyranoindol-3-ones (5), synthetic equivalents of indole-2,3-quinodimethanes, undergo Diels-Alder reaction with acetylenes and with benzyne to give carbazoles and benzocarbazoles respectively.
