
%0 Journal Article
%A Blunt, JW 
%A Ditzel, EJ 
%A Hartshorn, MP 
%A Hickey, BJ 
%A Johnstone, PK 
%A Munro, MHG 
%A Robinson, WT 
%T The acid-catalysed rearrangement of (8R, l3R)-8,17-epoxylabd-14-en-13-ol; X-ray structure analysis of a tetracyclic ether product
%J Australian Journal of Chemistry
%D 1981/11/01
%V 34
%N 11
%P 2475-2479
%K 
%R https://doi.org/10.1071/CH9812475
%U https://www.publish.csiro.au/paper/CH9812475 
%X The structure and stereochemistry of the tetracyclic ether (5) formed in the acid-catalysed rearrangement of (8R,13R)-8,17-epoxylabd-14-en-13-ol (3) is presented. Although vinyl group participation was involved it was by a non-biosynthetic route. 
