Document Detail


Highly enantioselective fluorescent recognition of serine and other amino acid derivatives.
MedLine Citation:
PMID:  20726589     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The BINOL-amino alcohol compound (S)-4 was found to conduct enantioselective fluorescent recognition of a serine derivative with an unprecedented high ef [enantioselective fluorescent enhancement = (I(D) - I(0))/(I(L) - I(0))] of 12.5. Both (S)-4 and (S)-5 are also found to be highly enantioselective fluorescent sensors for a number of other amino acid derivatives.
Authors:
Hai-Lin Liu; Hu-Ping Zhu; Xue-Long Hou; Lin Pu
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.    
Journal Detail:
Title:  Organic letters     Volume:  12     ISSN:  1523-7052     ISO Abbreviation:  Org. Lett.     Publication Date:  2010 Sep 
Date Detail:
Created Date:  2010-09-10     Completed Date:  2010-12-21     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  100890393     Medline TA:  Org Lett     Country:  United States    
Other Details:
Languages:  eng     Pagination:  4172-5     Citation Subset:  IM    
Affiliation:
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Ling Ling Rd, Shanghai 200032, China.
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MeSH Terms
Descriptor/Qualifier:
Amino Acids / chemistry*
Molecular Structure
Serine / chemistry*
Spectrometry, Fluorescence
Stereoisomerism
Chemical
Reg. No./Substance:
0/Amino Acids; 56-45-1/Serine

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


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