The first phase of the total synthesis of thiostrepton (1), a highly complex thiopeptide antibiotic, is described. After a brief introduction to the target molecule and its structural motifs, it is shown that retrosynthetic analysis of thiostrepton reveals compounds 23, 24, 26, 28, and 29 as potential key building blocks for the projected total synthesis. Concise and stereoselective constructions of all these intermediates are then described. The synthesis of the dehydropiperidine core 28 was based on a biosynthetically inspired aza-Diels-Alder dimerization of an appropriate azadiene system, an approach that was initially plagued with several problems which were, however, resolved satisfactorily by systematic investigations. The quinaldic acid fragment 24 and the thiazoline-thiazole segment 26 were synthesized by a series of reactions that included asymmetric and other stereoselective processes. The dehydroalanine tail precursor 23 and the alanine equivalent 29 were also prepared from the appropriate amino acids. Finally, a method was developed for the direct coupling of the labile dehydropiperidine key building block 28 to the more advanced and stable peptide intermediate 27 through capture with the highly reactive alanine equivalent 67 under conditions that avoided the initially encountered destructive ring contraction process.

Total synthesis of thiostrepton. Retrosynthetic analysis and construction of key building blocks / K. C., Nicolaou; Brian S., Safina; Mark, Zak; Sang Hyup, Lee; Marta, Nevalainen; Bella, Marco; Anthony A., Estrada; Christian, Funke; Frédéric J., Zecri; Stephan, Bulat. - In: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. - ISSN 0002-7863. - 127:31(2005), pp. 11159-11175. [10.1021/ja0529337]

Total synthesis of thiostrepton. Retrosynthetic analysis and construction of key building blocks

BELLA, Marco;
2005

Abstract

The first phase of the total synthesis of thiostrepton (1), a highly complex thiopeptide antibiotic, is described. After a brief introduction to the target molecule and its structural motifs, it is shown that retrosynthetic analysis of thiostrepton reveals compounds 23, 24, 26, 28, and 29 as potential key building blocks for the projected total synthesis. Concise and stereoselective constructions of all these intermediates are then described. The synthesis of the dehydropiperidine core 28 was based on a biosynthetically inspired aza-Diels-Alder dimerization of an appropriate azadiene system, an approach that was initially plagued with several problems which were, however, resolved satisfactorily by systematic investigations. The quinaldic acid fragment 24 and the thiazoline-thiazole segment 26 were synthesized by a series of reactions that included asymmetric and other stereoselective processes. The dehydroalanine tail precursor 23 and the alanine equivalent 29 were also prepared from the appropriate amino acids. Finally, a method was developed for the direct coupling of the labile dehydropiperidine key building block 28 to the more advanced and stable peptide intermediate 27 through capture with the highly reactive alanine equivalent 67 under conditions that avoided the initially encountered destructive ring contraction process.
2005
01 Pubblicazione su rivista::01a Articolo in rivista
Total synthesis of thiostrepton. Retrosynthetic analysis and construction of key building blocks / K. C., Nicolaou; Brian S., Safina; Mark, Zak; Sang Hyup, Lee; Marta, Nevalainen; Bella, Marco; Anthony A., Estrada; Christian, Funke; Frédéric J., Zecri; Stephan, Bulat. - In: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. - ISSN 0002-7863. - 127:31(2005), pp. 11159-11175. [10.1021/ja0529337]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/131563
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