Abstract
A general synthetic approach to enantiomerically pure 4-substituted has been developed which provides access to the 4-alkylamino-2, 4-dideoxy-L-r/zreo-pentopyranose components of the calicheamicins and esperamicins.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1369-1378 |
| Number of pages | 10 |
| Journal | Journal of Carbohydrate Chemistry |
| Volume | 14 |
| Issue number | 9 |
| DOIs | |
| State | Published - Dec 1 1995 |
ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
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Mash, E. A., Nimkar, S. K., & DeMoss, S. M. (1995). A synthesis of the 4-alkylamino-2, 4-dideoxy-l-thero-pentopyranose components of the calicheamicins and esperamicins. Journal of Carbohydrate Chemistry, 14(9), 1369-1378. https://doi.org/10.1080/07328309508005417