Document Detail


A simple quick route to fullerene amino acid derivatives.
MedLine Citation:
PMID:  20517578     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Two new fullerene amino acids have been prepared by dipolar addition to C(60) of either the Boc- or Fmoc-Nalpha-protected azido amino acids derived from phenylalanine and lysine. UV-visible and CV studies indicate the as prepared amino acids are a mixture of 5,6-open (major product) and 6,6-closed (minor product) derivatives that may be readily separated.
Authors:
T Amanda Strom; Andrew R Barron
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2010-06-02
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:  2010-06-23     Completed Date:  2010-09-28     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9610838     Medline TA:  Chem Commun (Camb)     Country:  England    
Other Details:
Languages:  eng     Pagination:  4764-6     Citation Subset:  IM    
Affiliation:
Richard E. Smalley Institute for Nanoscale Science and Technology, Center for Biological and Environmental Nanotechnology, and Department of Chemistry, Rice University, Houston, Texas 77005, USA.
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MeSH Terms
Descriptor/Qualifier:
Aza Compounds / chemistry
Electrochemical Techniques
Fullerenes / chemistry*
Lysine / chemistry*
Phenylalanine / chemistry*
Spectrophotometry, Ultraviolet
Chemical
Reg. No./Substance:
0/Aza Compounds; 0/Fullerenes; 56-87-1/Lysine; 63-91-2/Phenylalanine; 99685-96-8/fullerene C60

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


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