4.8 Article

Total synthesis of crisamicin A

Journal

ORGANIC LETTERS
Volume 10, Issue 14, Pages 3017-3020

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol800977n

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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 unique cis-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.

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