Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5280902 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
The first total synthesis of didmolamides A (1) and B (2) has been accomplished by the solid phase assembly of thiazole-containing amino acids and commercially available Fmoc-protected amino acids. The synthesis of didmolamide B was also achieved in high yield using solution phase peptide synthesis. The thiazole-containing amino acid composing 1 and 2 was synthesized by a MnO2 oxidation of a thiazoline, prepared from an Ala-Cys dipeptide using bis(triphenyl)oxodiphosphonium trifluoromethanesulfonate. The final macrolactamization was accomplished efficiently by PyBOP and DMAP in solution.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Shu-Li You, Jeffery W. Kelly,