Abstract
A "3+2+1" fragment condensation strategy to a precursor of the hexapeptide found in antibiotic A83586C is described. © 1994.
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CITATION STYLE
APA
Hale, K. J., Delisser, V. M., Yeh, L. K., Peak, S. A., Manaviazar, S., & Bhatia, G. S. (1994). Synthetic studies on the azinothricin family of antibiotics. 3. Enantioselective synthesis of a hexapeptide precursor for antitumour antibiotic A83586C. Tetrahedron Letters, 35(41), 7685–7688. https://doi.org/10.1016/S0040-4039(00)78375-4
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