Paper
Diastereoselective synthesis of vicinal amino alcohols.
Published Jun 14, 2012 · Oskari K. Karjalainen, A. Koskinen
Organic & biomolecular chemistry
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Abstract
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.
Study Snapshot
Key takeawayDiastereoselective synthesis of vicinal amino alcohols from amino acids offers a natural, inexpensive, and enantiopure starting material for natural products and pharmaceuticals, but diastereoselectivity remains a challenge.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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