Reddy, A. Bal ; Kumara Swamy, B. ; Yadav, Jhillu Singh (2016) A concise total synthesis of cleistenolide Tetrahedron: Asymmetry, 27 (16). pp. 788-790. ISSN 0957-4166
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Official URL: http://doi.org/10.1016/J.Tetasy.2016.06.012
Related URL: http://dx.doi.org/10.1016/J.Tetasy.2016.06.012
Abstract
A concise total synthesis of cleistenolide has been achieved from d-glucose. The synthesis of cleistenolide proceeds in six steps from d-glucose diacetonide in 42.5% overall yield. Selective benzoylation and Still-Gennari olefination are the key reactions involved in the synthesis.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| ID Code: | 135703 |
| Deposited On: | 10 Aug 2023 10:10 |
| Last Modified: | 10 Aug 2023 10:10 |
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