Synthesis of a new family of 2-ethylidene-[gamma]-unsaturated [delta]-amino esters via microwave activated Stille coupling
A simple approach to a new family of enantiomerically enriched polyunsaturated t-Boc-protected-δ-amino esters is described, via microwave promoted Stille coupling of (Z)-methyl-2-bromobutenoate with stannylated allylamines. The reaction conditions are mild and selective and disclose a simple way to...
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Veröffentlicht in: | Amino acids 2010-06, Vol.39 (1), p.175 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | A simple approach to a new family of enantiomerically enriched polyunsaturated t-Boc-protected-δ-amino esters is described, via microwave promoted Stille coupling of (Z)-methyl-2-bromobutenoate with stannylated allylamines. The reaction conditions are mild and selective and disclose a simple way to 1-substituted butenoates of defined geometry.[PUBLICATION ABSTRACT] |
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ISSN: | 0939-4451 1438-2199 |
DOI: | 10.1007/s00726-009-0392-y |