Ring-Rearrangement Metathesis of Substituted 2-Aminonorbornenes
Abstract In this report we describe the ring-rearrangement metathesis of 2-aminonorbornene derivatives. An 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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Veröffentlicht in: | Synlett 2007-07, Vol.2007 (11), p.1663-1666 |
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container_title | Synlett |
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creator | Nadany, Adam E. Mckendrick, John E. |
description | Abstract
In this report we describe the ring-rearrangement metathesis of 2-aminonorbornene derivatives. An efficient ruthenium-catalysed metathesis reaction occurs with a wide range of pendent alkenes and alkynes to generate bicyclic amines and amides. |
doi_str_mv | 10.1055/s-2007-982573 |
format | Article |
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In this report we describe the ring-rearrangement metathesis of 2-aminonorbornene derivatives. An efficient ruthenium-catalysed metathesis reaction occurs with a wide range of pendent alkenes and alkynes to generate bicyclic amines and amides.</abstract><doi>10.1055/s-2007-982573</doi><tpages>4</tpages></addata></record> |
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title | Ring-Rearrangement Metathesis of Substituted 2-Aminonorbornenes |
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