Jump to main content
Jump to site search

Issue 44, 2018
Previous Article Next Article

Synthetic studies on daphniglaucins

Author affiliations


The synthetic approach to the core framework of daphniglaucin-type Daphniphyllum alkaloids is described herein. The B–C ring was constructed via a Rh-catalyzed [3+2] cycloaddition. Continuous quaternary centers were installed through [3+2] cycloaddition and alkylation. The attempt to build the A–D ring motif using dipolar cycloaddition of azomethine ylides was extensively investigated.

Graphical abstract: Synthetic studies on daphniglaucins

Back to tab navigation

Supplementary files

Publication details

The article was received on 17 Apr 2018, accepted on 03 May 2018 and first published on 03 May 2018

Article type: Communication
DOI: 10.1039/C8CC03063D
Chem. Commun., 2018,54, 5554-5557

  •   Request permissions

    Synthetic studies on daphniglaucins

    Y. Qiu, J. Zhong, S. Du and S. Gao, Chem. Commun., 2018, 54, 5554
    DOI: 10.1039/C8CC03063D

Search articles by author