Total synthesis of isokidamycin |
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Authors: | O'Keefe B Michael Mans Douglas M Kaelin David E Martin Stephen F |
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Affiliation: | Department of Chemistry and Biochemistry, The University of Texas, Austin, Texas 78712, USA. |
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Abstract: | The synthesis of isokidamycin, which represents the first total synthesis of a bis-C-aryl glycoside natural product in the pluramycin family, has been completed. The synthesis features the use of a silicon tether as a disposable regiocontrol element in an intramolecular Diels-Alder reaction between a substituted naphthyne and a glycosyl furan and a subsequent O→C-glycoside rearrangement. |
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