Document Detail


Diastereoselective synthesis of vicinal amino alcohols.
MedLine Citation:
PMID:  22535485     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
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.
Authors:
Oskari K Karjalainen; Ari M P Koskinen
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Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-4-25
Journal Detail:
Title:  Organic & biomolecular chemistry     Volume:  -     ISSN:  1477-0539     ISO Abbreviation:  -     Publication Date:  2012 Apr 
Date Detail:
Created Date:  2012-4-26     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101154995     Medline TA:  Org Biomol Chem     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Affiliation:
Department of Chemistry, Aalto University School of Chemical Technology, P.O. Box 16100 (Kemistintie 1), FI-00076 Aalto, Finland. ari.koskinen@aalto.fi.
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