Chakraborty, Tushar Kanti ; Reddy, Vakiti Ramkrishna (2006) Studies directed towards the total synthesis of clavosolides: synthesis of an isomer of clavosolide A Tetrahedron Letters, 47 (13). pp. 2099-2102. ISSN 0040-4039
Full text not available from this repository.
Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...
Related URL: http://dx.doi.org/10.1016/j.tetlet.2006.01.130
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.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Clavosolides; Clavosolide A; Epoxide Opening; 2-Methyl-1; 3-diol; Diolide |
| ID Code: | 20529 |
| Deposited On: | 20 Nov 2010 14:22 |
| Last Modified: | 20 Nov 2010 14:22 |
Repository Staff Only: item control page
