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Ring-rearrangement metathesis of substituted 2-aminonorbornenes

Nadany, A.E. and McKendrick, J.E. (2007) Ring-rearrangement metathesis of substituted 2-aminonorbornenes. Synlett (11). pp. 1663-1666. ISSN 0936-5214

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To link to this item DOI: 10.1055/s-2007-982573

Abstract/Summary

In this report we describe the ring-rearrangement metathesis of 2-aminonorbornene derivatives. Ail efficient ruthenium-catalysed metathesis reaction Occurs with a wide range of pendent alkenes and alkynes to generate bicyclic amines and amides.

Item Type:Article
Refereed:Yes
Divisions:Interdisciplinary centres and themes > Chemical Analysis Facility (CAF) > Mass Spectrometry (CAF)
Faculty of Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry
ID Code:11522
Uncontrolled Keywords:metathesis, Diels-Alder reaction, piperidine alkaloids , REGIOSELECTIVE DOMINO METATHESIS, OLEFIN-METATHESIS, CLOSING METATHESIS, ENYNE METATHESIS, ALKYLIDENE COMPLEXES, NATURAL-PRODUCT, CATALYSTS, STRATEGY, (+)-STREPTAZOLIN, POLYMERIZATION

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