Srikrishna, A. ; Satyanarayana, G. ; Prasad, K. R. (2007) RCM-based approach to (±)-cuparene Synthetic Communications, 37 (9). pp. 1511-1516. ISSN 0039-7911
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Official URL: http://www.tandfonline.com/doi/abs/10.1080/0039791...
Related URL: http://dx.doi.org/10.1080/00397910701229214
Abstract
An efficient approach to the aromatic sesquiterpene cuparene has been described starting from the readily available β-ionone and employing a combination of epoxide rearrangement-based ring-contraction and ring-closing metathesis reactions as key steps.
Item Type: | Article |
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Source: | Copyright of this article belongs to Taylor and Francis Group. |
Keywords: | Cupranes; Epoxide Rearrangement; Metathesis; Quaternary Carbons; Terpene Synthesis |
ID Code: | 51559 |
Deposited On: | 28 Jul 2011 14:34 |
Last Modified: | 28 Jul 2011 14:34 |
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