Synthesis of Oligodeoxynucleotides by the Phosphite‐Triester Method Using Dimer Units and Different Phosphorous‐Protecting Groups
- 13 November 1985
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 68 (7) , 1907-1913
- https://doi.org/10.1002/hlca.19850680714
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Improvements in oligodeoxyribonucleotide synthesis: methyl N,N-dialkylphosphoramidite dimer units for solid support phosphite methodologyThe Journal of Organic Chemistry, 1984
- Improvements in the phosphotriester synthesis of deoxyribooligonucleotides - the use of hindered amines and a new isolation procedureTetrahedron Letters, 1982
- Selective N-deacylation of N,O-protected nucleosides by zinc bromideTetrahedron Letters, 1981
- Nucleosides and Nucleotides. Part 17. A simple preparation of protected deoxynucleoside‐3'‐phosphatesHelvetica Chimica Acta, 1981
- Synthesis of oligodeoxyribonucleotides on silica gel supportNucleic Acids Research, 1981
- Synthesis of the 3'-terminal decaribonucleoside nonaphosphate of yeast alanine transfer ribonucleic acidTetrahedron, 1980
- Oximate ion promoted unblocking of oligonucleotide phosphotriester intermediatesTetrahedron Letters, 1978
- Synthesis of oligoribonucleotides based on the facile cleavage of methyl phosphotriester intermediatesJournal of the American Chemical Society, 1977