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
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- United Kingdom
- INIS RN
- 27010135
- Subject category
- S38: RADIATION CHEMISTRY, RADIOCHEMISTRY AND NUCLEAR CHEMISTRY;
- Descriptors DEI
- ADENINES; CHEMICAL PREPARATION; LABELLED COMPOUNDS; LABELLING; NITROGEN 15; NUCLEOSIDES
- Descriptors DEC
- AMINES; ANTIMETABOLITES; AROMATICS; AZAARENES; DRUGS; HETEROCYCLIC COMPOUNDS; ISOTOPES; LIGHT NUCLEI; NITROGEN ISOTOPES; NUCLEI; NUCLEOTIDES; ODD-EVEN NUCLEI; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; PURINES; RIBOSIDES; STABLE ISOTOPES; SYNTHESIS