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
Hauptverfasser: Nadany, Adam E., Mckendrick, John E.
Format: Artikel
Sprache:eng
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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.
ISSN:0936-5214
1437-2096
DOI:10.1055/s-2006-948211