160983-67-5Relevant academic research and scientific papers
Transition-metal-free [3 + 3] annulation of indol-2-ylmethyl carbanions to nitroarenes. A novel synthesis of indolo[3,2-b]quinolines (quindolines)
Nowacki, Micha?,Wojciechowski, Krzysztof
, p. 194 - 202 (2018)
Indol-2-ylmethyl carbanions stabilized by alkoxycarbonyl, cyano or benzenesulfonyl groups react with nitroarenes to form σH-adducts, which in the presence of base (triethylamine or DBU) and trimethylchlorosilane transform into indolo[3,2-b]quinoline derivatives in moderate to good yields.
Organocatalyzed asymmetric synthesis of morphans
Bradshaw, Ben,Parra, Claudio,Bonjoch, Josep
supporting information, p. 2458 - 2461 (2013/06/27)
A general effective organocatalyzed synthesis of enantioenriched morphans with up to 92% ee was developed. The morphan scaffold was constructed in a one-pot tandem asymmetric organocatalyzed Michael addition followed by a domino Robinson annulation/aza-Michael intramolecular reaction sequence from easily available starting materials.
Intramolecular Diels-Alder Reactions of Pyranoindol-3-ones. Preparation of -Annelated Carbazoles
Moody, Christopher J.,Mprrell, Andrew I.
, p. 309 - 314 (2007/10/02)
The pyranoindol-3-ones (5), readily prepared from t-butyl indole-2-acetate (2) in three steps, undergo facile intramolecular Diels-Alder reaction on heating to give, after loss of carbon dioxide, the -annelated carbazoles (6).
