A rapid internucleotide bond formation for the phosphotriester approach by use of new condensing reagents
- PMID: 6522301
A rapid internucleotide bond formation for the phosphotriester approach by use of new condensing reagents
Abstract
Bis(2,4,6-trihalophenyl) phosphorochloridates (TCP and TBP) were found to be effective as condensing reagents for the rapid internucleotidic phoshotriester bond formation. The benzoyl group as the N3-imide protecting group of thymidine was also useful for prevention of the side reaction caused by the active condensing reagents.
Similar articles
-
Tris(2,4,6-tribromophenoxy)dichlorophosphorane as a condensing agent: a new type of activation of phosphodiester components in the phosphotriester method.Nucleic Acids Symp Ser. 1988;(19):17-20. Nucleic Acids Symp Ser. 1988. PMID: 3226914
-
A novel class of condensing reagents in phosphodiester oligodeoxyribonucleotides synthesis. Application of the constituents of free terminal carboxy oxytocine gene.Nucleic Acids Symp Ser. 1980;(7):23-37. Nucleic Acids Symp Ser. 1980. PMID: 7255170
-
Synthesis of nucleotide oligomer having amino group in the side chain of internucleotidic bond.Nucleic Acids Symp Ser. 1984;(15):97-100. Nucleic Acids Symp Ser. 1984. PMID: 6522302
-
Recent progress in oligonucleotide synthesis.Acta Biochim Pol. 1996;43(1):37-44. Acta Biochim Pol. 1996. PMID: 8790710 Review.
-
Protecting groups in oligonucleotide synthesis.Methods Mol Biol. 1994;26:1-71. doi: 10.1007/978-1-59259-513-6_1. Methods Mol Biol. 1994. PMID: 7508800 Review. No abstract available.
MeSH terms
Substances
LinkOut - more resources
Miscellaneous