| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 9564730 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
Chloramphenicol has been prepared in 45% overall yield; the key step is the synthesis of a selectively protected 1,2-diol from an epoxide in an aqueous medium.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Joshodeep Boruwa, Jagat C. Borah, Siddhartha Gogoi, Nabin C. Barua,