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Asymmetric total syntheses of callistrilones B, G and J

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Abstract

A very concise approach for the first asymmetric and scalable total syntheses of callistrilones B, G and J has been developed. These syntheses proceeded in only 3–4 steps from the commercially available (−)-α-phellandrene (8), without the need for protecting groups. The key feature of the syntheses was a biomimetic, diastereo- and regioselective oxidative [3 + 2] cycloaddition.

Graphical abstract: Asymmetric total syntheses of callistrilones B, G and J

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Publication details

The article was received on 04 Feb 2018, accepted on 14 Mar 2018 and first published on 15 Mar 2018


Article type: Research Article
DOI: 10.1039/C8QO00130H
Citation: Org. Chem. Front., 2018, Advance Article
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    Asymmetric total syntheses of callistrilones B, G and J

    L. Hu, M. Cheng, J. Cao, L. Zhong, Y. Hu, Y. Wang, L. Wang, W. Ye and C. Li, Org. Chem. Front., 2018, Advance Article , DOI: 10.1039/C8QO00130H

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