The methyl group as phosphate protecting group in nucleotide syntheses
- 31 December 1980
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 21 (9) , 861-864
- https://doi.org/10.1016/s0040-4039(00)71527-9
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Synthesis of oligoribonucleotides based on the facile cleavage of methyl phosphotriester intermediatesJournal of the American Chemical Society, 1977
- Synthesis of thymidine oligonucleotides by phosphite triester intermediatesJournal of the American Chemical Society, 1976
- Synthesis of Lactose-Operator Gene Fragments by the Improved Triester MethodCanadian Journal of Chemistry, 1974
- Internucleotide cleavage during unblocking in oligonucleotide synthesis by the phosphotriester approachTetrahedron Letters, 1974
- The tert-Butyldimethylsilyl Group as a Protecting Group in DeoxynucleosidesCanadian Journal of Chemistry, 1973
- Deoxy oligonucleotide synthesis via the triester methodThe Journal of Organic Chemistry, 1973
- Conformation and interaction of dinucleoside mono- and diphosphates. V. Syntheses and properties of adenine and thymine nucleoside alkyl phosphotriesters, the neutral analogs of dinucleoside monophosphatesJournal of the American Chemical Society, 1971
- Oligoribonucleotide Synthesis III. Synthesis of Trinucleotides Using a Stepwise Phosphotriester MethodCanadian Journal of Chemistry, 1971
- Convenient method for stepwise synthesis of oligothymidylate derivatives in large-scale quantitiesJournal of the American Chemical Society, 1967
- β.β.β‐Trichlor‐äthanol als Phosphorsäureschutzgruppe für NucleotideEuropean Journal of Inorganic Chemistry, 1967