| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279783 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
The total synthesis of clavosolide A, employing a radical-mediated route to build its substituted tetrahydropyran unit, a Yamaguchi reaction to construct the diolide aglycon and the Schmidt method for the final glycosidation step, revealed that the reported structure is an isomer of the natural product.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Tushar Kanti Chakraborty, Vakiti Ramkrishna Reddy,