The stereoselective synthesis of a novel aromatic peptide nucleic acid (APNA) oligomer
The synthesis of the thymine derivative (S)-50, was achieved in high enantiomeric purity (98% ee). The (R) enhanced enantiomer was also synthesized with moderate enantiomeric purity (46% ee). This acyclic pyrimidine analog ((S)-50) is a useful building block for the synthesis of a novel class of oli...
| Main Author: | |
|---|---|
| Format: | Others |
| Published: |
1997
|
| Online Access: | http://spectrum.library.concordia.ca/225/1/MQ25983.pdf Lunetta, Jacqueline F <http://spectrum.library.concordia.ca/view/creators/Lunetta=3AJacqueline_F=3A=3A.html> (1997) The stereoselective synthesis of a novel aromatic peptide nucleic acid (APNA) oligomer. Masters thesis, Concordia University. |
Internet
http://spectrum.library.concordia.ca/225/1/MQ25983.pdfLunetta, Jacqueline F <http://spectrum.library.concordia.ca/view/creators/Lunetta=3AJacqueline_F=3A=3A.html> (1997) The stereoselective synthesis of a novel aromatic peptide nucleic acid (APNA) oligomer. Masters thesis, Concordia University.