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
Hauptverfasser: Herold-Dublin, Marike, Liotta, Dennis C
Format: Artikel
Sprache:eng
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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.
ISSN:0008-4042
1480-3291
DOI:10.1139/v06-179