A simple method for N-acylation of adenosine and cytidine nucleosides using carboxylic acids activated In-Situ with carbonyldiimidazole
- 18 December 1995
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (51) , 9277-9280
- https://doi.org/10.1016/0040-4039(95)02011-d
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Synthesis and properties of oligonucleotides containing the mutagenic base O4-benzylthymidineBioorganic & Medicinal Chemistry, 1995
- On the rapid deprotection of synthetic oligonucleotides and analogsNucleic Acids Research, 1994
- Labile exocyclic amine protection of nucleosides in DNA, RNA and oligonucleotide analog synthesis facililating N-deacylation, minimizing depurination and chain degradationBiochimie, 1993
- Synthesis and duplex stability of oligodeoxynucleotides containing 6-mercaptopurineTetrahedron Letters, 1992
- The use of labile base protecting groups in oligoribonucleotide synthesisTetrahedron Letters, 1989
- The isopropoxyacetic group for convenient base protection during solid-support synthesis of oligodeoxyribonucleotides and their triester analogsNucleic Acids Research, 1988
- Transient protection: efficient one-flask syntheses of protected deoxynucleosidesJournal of the American Chemical Society, 1982
- Studies on Polynucleotides. XXIV.1 The Stepwise Synthesis of Specific Deoxyribopolynucleotides (4).2 Protected Derivatives of Deoxyribonucleosides and New Syntheses of Deoxyribonucleoside-3″ Phosphates3Journal of the American Chemical Society, 1963
- N,N'-Carbonyldiimidazole in Peptide Synthesis. III.1 A Synthesis of Isoleucine-5 Angiotensin II Amide-IThe Journal of Organic Chemistry, 1962
- N,N'-Carbonyldiimidazole, a New Peptide Forming Reagent1Journal of the American Chemical Society, 1960