Total synthesis of the C-3 – C-17 segment of boromycin
- 1 March 1983
- journal article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 61 (3) , 634-637
- https://doi.org/10.1139/v83-115
Abstract
The C-3 – C-17 segment of boromycin having five asymmetric centers was synthesized from D-arabinose and D-glucose as chiral precursors. Constitutional and stereochemical identity was established by comparison of the synthetic product with a sample obtained from the degradation of the antibiotic.Keywords
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