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Application of olefin metathesis for the synthesis of constrained beta-amino esters from norbornenes

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Nadany, A.E. and McKendrick, J.E. ORCID: https://orcid.org/0000-0003-2275-0569 (2006) Application of olefin metathesis for the synthesis of constrained beta-amino esters from norbornenes. Synlett (13). pp. 2139-2141. ISSN 0936-5214

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To link to this item DOI: 10.1055/s-2006-948211

Abstract/Summary

Synthesis of a number of novel, conformationally rigid beta-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.

Item Type:Article
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
ID Code:11520
Uncontrolled Keywords:metathesis, amino acids, Diels-Alder reactions, RING-CLOSING METATHESIS, DOMINO METATHESIS, CONVENIENT SYNTHESIS, DERIVATIVES, ANHYDRIDES, STRATEGY, POLYMERIZATION, LACTAMS, ACIDS
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