R-1-Phenylethylamine as chiral auxiliary in the diastereoselective synthesis of tetrahydro-3- carboline derivatives
Modified sodium borohydrides were used in the reduction of the imine moiety in compounds containing the (R)-1-arylethylamine motif as a chiral auxiliary. Diastereomeric products were formed with moderate to good stereoselectivity and were effectively separated by column chromatography. [PUBLICATION...
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Veröffentlicht in: | Canadian journal of chemistry 2007-12, Vol.85 (12), p.1033 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Modified sodium borohydrides were used in the reduction of the imine moiety in compounds containing the (R)-1-arylethylamine motif as a chiral auxiliary. Diastereomeric products were formed with moderate to good stereoselectivity and were effectively separated by column chromatography. [PUBLICATION ABSTRACT] |
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ISSN: | 0008-4042 1480-3291 |