Diastereoselective addition of chlorotitanium enolates of N-acyl thiazolidinethione to activated imines A novel synthesis of β-lactams
We report a novel methodology for preparing enantiomerically pure β-lactams, starting from nitriles in diastereomeric ratios up to 10:1. The power of the methodology was demonstrated by the efficient synthesis of the cholesterol absorption inhibitor SCH 48462 .Key words: β-lactam, N-metalloaldimine,...
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Veröffentlicht in: | Canadian journal of chemistry 2006-12, Vol.84 (12), p.1696-1699 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | We report a novel methodology for preparing enantiomerically pure β-lactams, starting from nitriles in diastereomeric ratios up to 10:1. The power of the methodology was demonstrated by the efficient synthesis of the cholesterol absorption inhibitor
SCH 48462
.Key words: β-lactam, N-metalloaldimine, titanium Lewis acids, cholesterol absorption inhibitor. |
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ISSN: | 0008-4042 1480-3291 |
DOI: | 10.1139/v06-179 |