The synthesis of angularly fused tricyclic compoundsvia tandem ring closing metathesis reactions

Martin J. Bassindale; Andrew S. Edwards; Peter Hamley; Harry Adams; Joseph P. A. Harrity

doi:10.1039/B002136I

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The synthesis of angularly fused tricyclic compounds via tandem ring closing metathesis reactionsElectronic supplementary information (ESI) available: general experimental and synthetic and spectral data for the new compounds. See http://www.rsc.org/suppdata/cc/b0/b002136i/

Martin J. Bassindale,^a Andrew S. Edwards,^a Peter Hamley,^b Harry Adams^a and Joseph P. A. Harrity*^a

Author affiliations

* Corresponding authors

^a Department of Chemistry, University of Sheffield, Brook Hill, Sheffield, UK
E-mail: j.harrity@sheffield.ac.uk

^b Department of Medicinal Chemistry, AstraZeneca Research and Development, Charnwood, Bakewell Road, Loughborough, UK

Abstract

A novel and highly efficient approach to angularly fused tricycles has been developed through the employment of selective tandem ring closing metathesis reactions.

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Article information

DOI: https://doi.org/10.1039/B002136I
Article type: Communication
Submitted: 14 Mar 2000
Accepted: 03 May 2000
First published: 25 May 2000

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Chem. Commun., 2000, 1035-1036

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The synthesis of angularly fused tricyclic compounds via tandem ring closing metathesis reactions

M. J. Bassindale, A. S. Edwards, P. Hamley, H. Adams and J. P. A. Harrity, Chem. Commun., 2000, 1035 DOI: 10.1039/B002136I

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