| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5288649 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
The total synthesis of (â)-clavosolide A is achieved employing a radical-mediated route to build the substituted tetrahydropyran unit, a Yamaguchi reaction to construct the diolide aglycon and the Schmidt method for the final glycosidation step.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Tushar Kanti Chakraborty, Vakiti Ramkrishna Reddy, Amit Kumar Chattopadhyay,