Diastereoselective synthesis of vicinal amino alcohols

The vicinal amino alcohol is a common motif in natural products and pharmaceuticals. Amino acids constitute a natural, inexpensive, and enantiopure choice of starting material for the synthesis of such functionalities. However, the matters concerning diastereoselectivity are not obvious. This Perspe...

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Veröffentlicht in:Organic & biomolecular chemistry 2012-06, Vol.1 (22), p.4311-4326
Hauptverfasser: Karjalainen, Oskari K, Koskinen, Ari M. P
Format: Artikel
Sprache:eng
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Zusammenfassung:The vicinal amino alcohol is a common motif in natural products and pharmaceuticals. Amino acids constitute a natural, inexpensive, and enantiopure choice of starting material for the synthesis of such functionalities. However, the matters concerning diastereoselectivity are not obvious. This Perspective takes a look in the field of diastereoselective synthesis of vicinal amino alcohols starting from amino acids using various methods. In this era of enantioselective catalysis, diastereoselective synthesis still remains a central objective. In this Perspective the general issues determining diastereoselectivity in the synthesis of vicinal amino alcohols are discussed.
ISSN:1477-0520
1477-0539
DOI:10.1039/c2ob25357g