Document Detail


Efficient palladium-catalyzed cross-coupling of highly acidic substrates, nitroacetates.
MedLine Citation:
PMID:  22263870     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Palladium-catalyzed cross-coupling conditions were developed that efficiently afford 2-aryl-2-nitroacetates from aryl bromides and the very acidic nitroacetates.
Authors:
Alison E Metz; Simon Berritt; Spencer D Dreher; Marisa C Kozlowski
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.     Date:  2012-01-20
Journal Detail:
Title:  Organic letters     Volume:  14     ISSN:  1523-7052     ISO Abbreviation:  Org. Lett.     Publication Date:  2012 Feb 
Date Detail:
Created Date:  2012-02-03     Completed Date:  2012-05-04     Revised Date:  2014-06-24    
Medline Journal Info:
Nlm Unique ID:  100890393     Medline TA:  Org Lett     Country:  United States    
Other Details:
Languages:  eng     Pagination:  760-3     Citation Subset:  IM    
Copyright Information:
© 2012 American Chemical Society
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MeSH Terms
Descriptor/Qualifier:
Acetates / chemistry*
Catalysis
Hydrogen-Ion Concentration
Molecular Structure
Palladium / chemistry*
Grant Support
ID/Acronym/Agency:
1S10RR022442/RR/NCRR NIH HHS; 1S10RR023444/RR/NCRR NIH HHS; R01 GM087605/GM/NIGMS NIH HHS; R01 GM087605-02/GM/NIGMS NIH HHS; R01GM087605/GM/NIGMS NIH HHS
Chemical
Reg. No./Substance:
0/Acetates; 5TWQ1V240M/Palladium; 625-75-2/nitroacetic acid
Comments/Corrections

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