Yadav, J. S. ; Goreti, Rajendar ; Pabbaraja, Srihari ; Sridhar, B. (2013) Short Route to Platencin Organic Letters, 15 (14). pp. 3782-3785. ISSN 1523-7060
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Official URL: http://doi.org/10.1021/ol401760e
Related URL: http://dx.doi.org/10.1021/ol401760e
Abstract
The synthesis of the complex tricyclic core of the terpenoid antibiotic platencin is achieved in a concise, protecting group-free and stereoselective manner. A flexible approach that highlights the intramolecular aldol reaction as the key step toward the construction of the bicyclo[2,2,2]octane ring from an angular allyl decalone in both the trans-fused and the cis-fused forms is demonstrated.
Item Type: | Article |
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Source: | Copyright of this article belongs to American Chemical Society. |
ID Code: | 135732 |
Deposited On: | 11 Aug 2023 08:51 |
Last Modified: | 11 Aug 2023 08:51 |
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