Isocomplestatin:  Total Synthesis and Stereochemical Revision

A Pd-mediated method for preparation of the strained macrocyclic moiety of complestatins is disclosed. Through stereoselective synthesis of model macrocycles and the S atropisomer of complestatin, the stereochemical identity of the anti-HIV agent complestatin is established. Investigations described...

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Veröffentlicht in:Journal of the American Chemical Society 2005-05, Vol.127 (20), p.7334-7336
Hauptverfasser: Shinohara, Toshio, Deng, Hongbo, Snapper, Marc L, Hoveyda, Amir H
Format: Artikel
Sprache:eng
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Zusammenfassung:A Pd-mediated method for preparation of the strained macrocyclic moiety of complestatins is disclosed. Through stereoselective synthesis of model macrocycles and the S atropisomer of complestatin, the stereochemical identity of the anti-HIV agent complestatin is established. Investigations described herein illustrate that the compound previously reported as isocomplestatin is the same as complestatin. Thus, the S atropisomer of complestatin is the true isocomplestatin and has not been isolated as a natural product.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja051790l