Application of Olefin Metathesis for the Synthesis of Constrained β-Amino Esters from Norbornenes
Abstract Synthesis of a number of novel, conformationally rigid β-amino esters has been achieved via a tandem olefin metathesis reaction. The starting materials are readily accessible from the Diels-Alder adduct between cyclopentadiene and maleic anhydride.
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Veröffentlicht in: | Synlett 2006-08, Vol.2006 (13), p.2139-2141 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Abstract
Synthesis of a number of novel, conformationally rigid β-amino esters has been achieved via a tandem olefin metathesis reaction. The starting materials are readily accessible from the Diels-Alder adduct between cyclopentadiene and maleic anhydride. |
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ISSN: | 0936-5214 1437-2096 |
DOI: | 10.1055/s-2006-948211 |