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 |
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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. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/c2ob25357g |