Synlett 1997; 1997(1): 123-125
DOI: 10.1055/s-1997-695
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Synthesis of Hydroxylated Pyrrolizidines Related to Alexine using Cycloaddition Reactions of Functionalized Cyclic Nitrones

Adrian Hall, Kevin P. Meldrum, Patrick R. Therond, Richard H. Wightman*
  • *Department of Chemistry, Heriot-Watt University, Riccarton, Edinburgh EH14 4AS, U.K.
Further Information

Publication History

Publication Date:
22 March 2004 (online)

Cycloaddition reactions of the functionalized Δ1-pyrroline-N-oxides 10 and 19 have been used to prepare the hydroxylated pyrrolizidines 6 and 7 respectively, which are related to the natural products alexine and australine.

    >