Nagaraju, Chinta ; Prasad, Kavirayani R. (2014) An unusual ring-contraction/rearrangement sequence for making functionalized di- and triquinanes Angewandte Chemie International Edition, 53 (41). pp. 10997-11000. ISSN 1433-7851
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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/anie.20...
Related URL: http://dx.doi.org/10.1002/anie.201407680
Abstract
A novel ring contraction/rearrangement sequence leading to functionalized 2,8-oxymethano-bridged di- and triquinane compounds is observed in the reaction of various substituted 1-methyl-4-isopropenyl-6-oxabicylo[3.2.1]octan-8-ones with Lewis acids. The reaction is novel and is unprecedented for the synthesis of di- and triquinane frameworks.
Item Type: | Article |
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Source: | Copyright of this article belongs to John Wiley and Sons, Inc. |
Keywords: | Gold; Natural Products; Rearrangement; Ring Contraction; Synthetic Methods |
ID Code: | 105621 |
Deposited On: | 21 Dec 2017 12:01 |
Last Modified: | 21 Dec 2017 12:01 |
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