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Nadany, A.E. and McKendrick, J.E. 
ORCID: https://orcid.org/0000-0003-2275-0569
(2007)
Ring-rearrangement metathesis of substituted 2-aminonorbornenes.
Synlett (11).
pp. 1663-1666.
ISSN 0936-5214
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.
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| Item Type | Article |
| URI | https://reading-clone.eprints-hosting.org/id/eprint/11522 |
| Identification Number/DOI | 10.1055/s-2007-982573 |
| Refereed | Yes |
| Divisions | Interdisciplinary centres and themes > Chemical Analysis Facility (CAF) > Mass Spectrometry (CAF) Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry |
| 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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