32.Total Synthesis of Crisamicin A

Z. T. Li, Y. X. Gao, Y. F.  Tang, M. J. Dai, G. X. Wang, Z. G. Wang* and Z. Yang*

Org. Lett., 2008, 10, 3017.

Stereoselective total synthesis of natural product crisamicin A (1) was accomplished for the first time via the Pd/TMTU-catalyzed alkoxycarbonylative annulation to generate a uniquecis-pyran-fused lactone, an intermolecular Diels−Alder reaction to construct the pyranonaphthoquinone unit, and a novel Pd−thiourea pincer complex-catalyzed homocoupling of functionalized naphthoquinones.