80757-41-1Relevant academic research and scientific papers
A new synthetic route to indoloquinones: Formal synthesis of ellipticine
Mal, Dipakranjan,Senapati, Bidyut K.,Pahari, Pallab
, p. 994 - 996 (2005)
The anionic [4+2] cycloaddition of furoindolones with arynes and quinol ethers is introduced as an efficient strategy for the synthesis of indoloquinones. The utility of the strategy is exemplified by a very short synthesis of elipticine.
Anionic [4+2] cycloaddition strategy in the regiospecific synthesis of carbazoles: formal synthesis of ellipticine and murrayaquinone A
Mal, Dipakranjan,Senapati, Bidyut Kumar,Pahari, Pallab
, p. 3768 - 3781 (2008/02/01)
Anionic [4+2] cycloaddition of furoindolones (e.g., 7 and 10) has been developed as an effective means to the synthesis of carbazoles. This reaction has been shown to be feasible with a wide variety of Michael acceptors to give carbazoles and fused carbaz
