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Title: Stereocontrolled total synthesis of pancratistatin. Author: Kim S, Ko H, Kim E, Kim D. Journal: Org Lett; 2002 Apr 18; 4(8):1343-5. PubMed ID: 11950358. Abstract: A new total synthesis of the antitumor alkaloids, pancratistatin (1), has been accomplished from readily available staring materials. The Claisen rearrangement of dihydropyranethylene 5 was employed to construct the A and C rings. Stereo- and regiocontrolled functional group interchange, such as iodolactonization, dihydroxylations, and a cyclic sulfate elimination reaction, allows for the production of the target natural product. [reaction: see text][Abstract] [Full Text] [Related] [New Search]