Jump to main content
Jump to site search

Issue 22, 2014
Previous Article Next Article

A novel synthetic approach to the bicyclo[5.3.1]undecan-11-one framework of vinigrol

Author affiliations

Abstract

The first synthetic attempt commencing from an eight-membered ring to approach the [5.3.1] bicyclic core of vinigrol has demonstrated the feasibility of using the conformational bias of the cyclooctane-ring system to realize highly diastereoselective reactions. The synthetic potential of the newly disclosed access to in/out isomerism may stimulate broader interests.

Graphical abstract: A novel synthetic approach to the bicyclo[5.3.1]undecan-11-one framework of vinigrol

Back to tab navigation
Please wait while Download options loads

Supplementary files

Publication details

The article was received on 07 Jan 2014, accepted on 11 Feb 2014 and first published on 12 Feb 2014


Article type: Communication
DOI: 10.1039/C4OB00046C
Citation: Org. Biomol. Chem., 2014,12, 3562-3566
  •   Request permissions

    A novel synthetic approach to the bicyclo[5.3.1]undecan-11-one framework of vinigrol

    X. Wang, Y. Lu, J. Wang, X. Wang, H. Yao, G. Lin and B. Sun, Org. Biomol. Chem., 2014, 12, 3562
    DOI: 10.1039/C4OB00046C

Search articles by author