%0 Journal Article
%@ 0040-4039
%A Ueda, M
%A Walczak, MAA
%A Wipf, P
%D 2008
%F pittir:19251
%J Tetrahedron Letters
%N 41
%P 5986 - 5989
%T Formal Alder-ene reaction of a bicyclo[1.1.0]butane in the synthesis of the tricyclic quaternary ammonium core of daphniglaucins
%U http://d-scholarship-dev.library.pitt.edu/19251/
%V 49
%X A tricyclic substructure of the tetracyclic nitrogen core of the daphniglaucins was formed by an oxidative activation of the allyl side chain of a bicyclo[1.1.0]butylmethylamine, a spontaneous intramolecular formal Alder-ene reaction, and a selective cyclization of a triol intermediate. © 2008 Elsevier Ltd. All rights reserved.