Synthetic studies of superstolide A: a carbohydrate based synthesis of the C21-C26 segment
| Title | Synthetic studies of superstolide A: a carbohydrate based synthesis of the C21-C26 segment |
| Publication Type | Journal Article |
| Year of Publication | 2010 |
| Authors | Pal, R, Rahaman, H, Mohapatra, DK, Gurjar, MK |
| Journal | Letters in Organic Chemistry |
| Volume | 7 |
| Issue | 8 |
| Pagination | 657-660 |
| Date Published | DEC |
| ISSN | 1570-1786 |
| Keywords | Chiral pool, Potent cytotoxic, Regioselective epoxide opening, Stereoselective hydroboration-oxidation, Superstolide A |
| Abstract | The synthesis of C21-C26 fragment of superstolide A, starting from D-glucose diacetonide, involving regioselective ring opening of epoxide by Grignard reagent and regioselective stereospecefic hydroboration oxidation has been described. |
| DOI | 10.2174/157017810793811704 |
| Type of Journal (Indian or Foreign) | Foreign |
| Impact Factor (IF) | 0.785 |
Divison category:
Organic Chemistry