@article{345,
  author = {P. Molnár and J. Deli and E. Osz and Ferenc Zsila and Miklós Simonyi and G. Tóth},
  title = {Confirmation of the absolute (3R,3 S,6 R)-configuration of (all-E)-3 -epilutein},
  abstract = {Circular dichroism (CD) spectroscopy was used to distinguish between the isomeric (all-E)-configured 3 -epilutein (2) and 6 -epilutein (8) to establish the absolute configuration of epilutein samples of different (natural and semisynthetic) origin, including samples of 2 obtained from thermally processed sorrel. Thus, the CD data of lutein (1) and epilutein samples (2) were compared. Our results unambiguously confirmed the (3R,3 S,6 R)- configuration of all epilutein samples. Compound 2 was thoroughly characterized, and its 13C-NMR data are published herewith for the first time.},
  year = {2004},
  journal = {Helvetica Chimica Acta},
  volume = {87},
  pages = {2159-2168},
  month = {2004},
  url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-4644309094&partnerID=40&md5=434657a85824e8587c4d5c66ba0051a5},
  note = {Cited By :11Export Date: 25 February 2016},
}