Document Detail


Catalytic enantioselective aldol additions of alpha-isothiocyanato imides to alpha-ketoesters.
MedLine Citation:
PMID:  20485801     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A readily available bifunctional thiourea catalyst promotes aldol additions of alpha-isothiocyanato imides to alpha-ketoesters under mild reaction conditions to form beta-hydroxy-alpha-amino acid derivatives with high levels of enantioselectivity.
Authors:
Matthew K Vecchione; Le Li; Daniel Seidel
Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, Non-P.H.S.     Date:  2010-05-19
Journal Detail:
Title:  Chemical communications (Cambridge, England)     Volume:  46     ISSN:  1364-548X     ISO Abbreviation:  Chem. Commun. (Camb.)     Publication Date:  2010 Jul 
Date Detail:
Created Date:  2010-06-17     Completed Date:  2010-09-13     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9610838     Medline TA:  Chem Commun (Camb)     Country:  England    
Other Details:
Languages:  eng     Pagination:  4604-6     Citation Subset:  IM    
Affiliation:
Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, 610 Taylor Road, Piscataway, New Jersey 08854, USA.
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MeSH Terms
Descriptor/Qualifier:
Aldehydes / chemistry*
Amino Acids / chemical synthesis*,  chemistry
Catalysis
Crystallography, X-Ray
Esters / chemistry*
Imides / chemistry*
Ketones / chemistry*
Models, Molecular
Molecular Structure
Stereoisomerism
Thiourea / chemistry*
Chemical
Reg. No./Substance:
0/Aldehydes; 0/Amino Acids; 0/Esters; 0/Imides; 0/Ketones; 62-56-6/Thiourea

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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