Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance work on Wednesday 27th March 2019 from 11:00 AM to 1:00 PM (GMT).

During this time our website performance may be temporarily affected. We apologise for any inconvenience this might cause and thank you for your patience.


Issue 9, 2018
Previous Article Next Article

Asymmetric total syntheses of callistrilones B, G and J

Author affiliations

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

Back to tab navigation

Supplementary files

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., 2018,5, 1506-1510

  •   Request permissions

    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, 5, 1506
    DOI: 10.1039/C8QO00130H

Search articles by author

Spotlight

Advertisements