Phosphorylating agent for the synthesis of oligonucleotide with aliphatic amino group at 5′ end
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (23) , 2611-2614
- https://doi.org/10.1016/s0040-4039(00)96161-6
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- [57] Sequencing end-labeled DNA with base-specific chemical cleavagesPublished by Elsevier ,2004
- A novel method for the introduction of an aliphatic primary amino group at the 5′ terminus of synthetic oligonucleotidesTetrahedron Letters, 1986
- Fluorescence detection in automated DNA sequence analysisNature, 1986
- Efficient methods for attaching non-radioactive labels to the 5′ ends of synthetic oligodeoxyribonucleotidesNucleic Acids Research, 1986
- Chemical synthesis of deoxyribonucleotides containing deoxyadenosine at the 3'-end on a polystyrene polymer support.CHEMICAL & PHARMACEUTICAL BULLETIN, 1985
- The synthesis of oligonucleotides containing an aliphatic amino group at the 5′ terminus: synthesis of fluorescent DNA primers for use in DNA sequence analysisNucleic Acids Research, 1985
- Use of trichlorodimethylethyl as a protecting group and tributylphosphine as a deprotecting agent in oligonucleotide synthesisJournal of the American Chemical Society, 1982
- Arylsulfonyl chlorides in the presence of N-methylimidazole as efficient condensing reagents in phosphotriester oligonucleotide synthesisTetrahedron Letters, 1982
- DNA sequencing with chain-terminating inhibitorsProceedings of the National Academy of Sciences, 1977