Document Detail

A simple quick route to fullerene amino acid derivatives.
MedLine Citation:
PMID:  20517578     Owner:  NLM     Status:  MEDLINE    
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.
T Amanda Strom; Andrew R Barron
Related Documents :
6252738 - Conformational changes of hemoproteins as evidenced by second derivative spectroscopy o...
2764508 - Vinblastine-c4 alkyl maleoyl and amino acid maleoyl derivatives: i. chemistry and physi...
18961418 - Analytical chemistry of the sulphur acids.
4082728 - Acetohydroxyacid synthase inhibitors: n-phthalyl-l-valine anilide and related compounds.
4346428 - Quantitation of rna tumor viruses and viruslike particles in human milk by hybridizatio...
21627968 - Structure-activity relationships influencing lipid-induced changes in eif2α phosphoryl...
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    
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.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Aza Compounds / chemistry
Electrochemical Techniques
Fullerenes / chemistry*
Lysine / chemistry*
Phenylalanine / chemistry*
Spectrophotometry, Ultraviolet
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

Previous Document:  Back cover.
Next Document:  Enantioselective total synthesis of plakotenin, a cytotoxic metabolite from Plakortis sp.