Anionic [4+2] cycloaddition strategy in the regiospecific synthesis of carbazoles: formal synthesis of ellipticine and murrayaquinone A

作者：Mal Dipakranjan^*; Senapati Bidyut Kumar; Pahari Pallab

来源：Tetrahedron, 2007, 63(18): 3768-3781.

DOI：10.1016/j.tet.2007.02.060

• carbazole quinone
• anionic cycloaddition
• furoindolone

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 carbazoles in good yields. The scope and limitations of the reaction have been briefly studied. The nature of N-protection of the furoindolones (cf. 7) plays a major role in the success of annulation.

• 出版日期2007-4-30