A novel method for the introduction of an aliphatic primary amino group at the 5′ terminus of synthetic oligonucleotides
- 31 December 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (34) , 3991-3994
- https://doi.org/10.1016/s0040-4039(00)84892-3
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Nonenzymatic sequence-specific cleavage of single-stranded DNA.Proceedings of the National Academy of Sciences, 1985
- Chemical and enzymatic biotin-labeling of oligodeoxyribonucleotidesNucleic Acids Research, 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
- Polymer support oligonucleotide synthesis XVIII1.2): use ofβ-cyanoethyi-N,N-dialkylamino-/N-morpholino phosphoramidite of deoxynucleosides for the synthesis of DNA fragments simplifying deprotection and isolation of the final productNucleic Acids Research, 1984
- An improved syringe technique for the preparation of oligonucleotides of defined sequenceTetrahedron Letters, 1983
- Biotin and fluorescent labeling of RNA using T4 RNA ligaseNucleic Acids Research, 1983
- Improvements in the phosphoramidite procedure for the synthesis of oligodeoxyribonucleotidesNucleic Acids Research, 1983
- Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesisTetrahedron Letters, 1981
- Preparation of a porous microparticulatee anion-exchange chromatography support for proteinsJournal of Chromatography A, 1979
- Mechanism of hydrolysis of phosphorylethanolamine triesters. Multiple catalytic effects of an intramolecular amino groupJournal of the American Chemical Society, 1979