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  4. A Highly Enantio-Selective Hexitol Nucleic Acid Template for Nonenzymic Oligoguanylate Synthesis
 
research article

A Highly Enantio-Selective Hexitol Nucleic Acid Template for Nonenzymic Oligoguanylate Synthesis

Kozlov, Igor A.
•
Politis, Panagiotis K.
•
Pitsch, Stefan  
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1999
Journal of the American Chemical Society

The authors compare the enantiomeric cross-inhibition of D- and L-guanosine 5'-phosphoro-2-methyl-imidazole (I) polymn. on C10 (RNA), dC10 (DNA), or hC10 (hexitol nucleic acid) (II). RNA or DNA templates catalyze efficient oligomerization of D-I, with a strong enantiomeric cross-inhibition by L-I, but II shows efficient oligomerization of D-I with a less sever cross-inhibition, resulting in G6-9 polymers, thus showing that efficient selection of one optical isomer from a racemic mixt. of nucleotides during nonenzymic oligo-nucleotide synthesis on an analog of a nucleic acid template is possible, which may be of relevance to prebiotic conditions. [on SciFinder (R)]

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Type
research article
DOI
10.1021/ja9836489
Author(s)
Kozlov, Igor A.
Politis, Panagiotis K.
Pitsch, Stefan  
Herdewijn, Piet
Orgel, Leslie E.
Date Issued

1999

Published in
Journal of the American Chemical Society
Volume

121

Issue

5

Start page

1108

End page

1109

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCAN  
Available on Infoscience
February 27, 2006
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/225876
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