Chakraborty, Tushar Kanti ; Reddy, Vakiti Ramkrishna ; Gajula, Praveen Kumar (2008) Total synthesis of clavosolide A Tetrahedron, 64 (22). pp. 5162-5167. ISSN 00404020
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Official URL: http://doi.org/10.1016/j.tet.2008.03.039
Related URL: http://dx.doi.org/10.1016/j.tet.2008.03.039
Abstract
For the total synthesis of (−)-clavosolide A described herein, a Schmidt glycosidation reaction was used to attach the sugar moiety at an early stage in the synthesis to the 4-hydroxy group of the substituted tetrahydropyran unit of the molecule, which itself was built following a Ti(III)-mediated method developed by us earlier, and at the end, it was the Yamaguchi reaction that was successfully employed for the cyclodimerization of the two halves of the molecule leading to its total synthesis.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Ltd |
| Keywords: | Clavosolides;Clavosolide A;Epoxide opening;2-Methyl-1,3-diol;Diolide |
| ID Code: | 131169 |
| Deposited On: | 05 Dec 2022 05:42 |
| Last Modified: | 05 Dec 2022 05:42 |
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