Scope and Limitations of Optical Pure Hydantoins as Chiral Auxiliaries in Asymmetric Mannich Reactions

The Mannich reaction of various 5-substituted and N-acyl substituted chiral hydantoins with a series of aldimines smoothly occurred with full stereochemical control. These Mannich adducts have been cleaved by alcoholysis to afford several synthetically useful chiral building blocks like β-amino este...

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Veröffentlicht in:Chemical research in Chinese universities 2016-04, Vol.32 (2), p.219-225
Hauptverfasser: Chen, Feng, Lu, Cuifen, Nie, Junqi, Chen, Zuxing, Yang, Guichun
Format: Artikel
Sprache:eng
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Zusammenfassung:The Mannich reaction of various 5-substituted and N-acyl substituted chiral hydantoins with a series of aldimines smoothly occurred with full stereochemical control. These Mannich adducts have been cleaved by alcoholysis to afford several synthetically useful chiral building blocks like β-amino esters and β-lactams in good yields and in enantiopure form.
ISSN:1005-9040
2210-3171
DOI:10.1007/s40242-016-5273-9