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Total synthesis, stereochemical reassignment, and absolute configuration of chlorofusin.
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Total synthesis, assignment of absolute stereochemistry, and structural revision of chlorofusin.
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Solid-phase synthesis of chlorofusin analogues.
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First total synthesis and stereochemical revision of laxaphycin B and its extension to lyngbyacyclamide A.
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Natural product MDM2 inhibitors: anticancer activity and mechanisms of action.
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Evaluation of Chlorofusin, its Seven Chromophore Diastereomers, and Key Analogues.
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Synthesis of the Chlorofusin Cyclic Peptide.
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Total synthesis of chlorofusin, its seven chromophore diastereomers, and key partial structures.
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本文引用的文献

1
Total synthesis, assignment of absolute stereochemistry, and structural revision of chlorofusin.
J Am Chem Soc. 2007 May 23;129(20):6400-1. doi: 10.1021/ja072225g. Epub 2007 May 2.
2
Synthesis of the azaphilones using copper-mediated enantioselective oxidative dearomatization.
J Am Chem Soc. 2005 Jul 6;127(26):9342-3. doi: 10.1021/ja052049g.
4
Synthesis of the chlorofusin cyclic peptide: assignment of the asparagine stereochemistry.
Org Lett. 2003 Dec 25;5(26):5047-50. doi: 10.1021/ol036083g.
6
Binding of an inhibitor of the p53/MDM2 interaction to MDM2.
Chem Commun (Camb). 2003 Feb 7(3):316-7. doi: 10.1039/b211889k.
7

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