Published July 1995 | Version v1
Journal article

An improved synthesis of [amino-15N]adenine; useful in the large scale synthesis of 2'-deoxy[amino-15N]adenosine

  • 1. Furman Univ., Greenville, SC (United States). Dept. of Chemistry
  • 2. Los Alamos National Lab., NM (United States)
  • 3. Wesleyan Univ., Middletown, CT (United States). Dept. of Molecular Biology and Biochemistry

Description

The synthesis of 15N labeled nucleic acids has seen increased utility for the probing of local interactions in polynucleotides by multinuclear and multidimensional nuclear magnetic resonance spectroscopy. Interest in these labeled molecules has been stimulated by new methods which allow for the generation of significant quantities of labeled nucleosides and, as a consequence, synthetic DNA oligomers. We have been interested in the construction of purine derived 2'-deoxynucleosides which are specifically labeled at multiple positions. To accomplish this task our approach required the synthesis of a large quantity of 2'-deoxy[amino-15N]adenosine, which we viewed as a common precursor, for a series of multiply labeled purine 2'-deoxynucleosides. (author)

Additional details

Publishing Information

Journal Title
Journal of Labelled Compounds and Radiopharmaceuticals
Journal Volume
36
Journal Issue
7
Journal Page Range
p. 631-635.
ISSN
0362-4803
CODEN
JLCRD4