Facile methods to recycle nucleosides during solid phase synthesis of oligonucleotides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Advances in the Synthesis of Oligonucleotides by the Phosphoramidite Approach
2. Oligodeoxynucleoside methylphosphonates: synthesis and enzymic degradation
3. A new and versatile approach to the preparation of valuable deoxynucleoside 3′-phosphite intermediates
4. 2-cyanoethyl nucleoside 3′-phosphonates as a novel starting materials for oligonucleotide synthesis
5. Kinetic Characterization of Ribonuclease-Resistant 2′-Modified Hammerhead Ribozymes
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1. 3‘-H-Phosphonate Synthesis of Chiral Benzo[a]pyrene Diol Epoxide Adducts at N2 of Deoxyguanosine in Oligonucleotides;Chemical Research in Toxicology;2007-01-12
2. Nucleoside recovery in DNA and RNA synthesis;Tetrahedron Letters;1999-12
3. The first example of sequence-specific non-uniformly 13C5 labelled RNA: Synthesis of the 29mer HIV-1 TAR RNA with 13C Relaxation Window;Tetrahedron;1999-05
4. Synthesis of Oligonucleotides Containing 2?-Deoxyisoguanosine and 2?-Deoxy-5-methylisocytidine Using Phosphoramidite Chemistry;Helvetica Chimica Acta;1998
5. N3‘→P5‘ Oligodeoxyribonucleotide Phosphoramidates: A New Method of Synthesis Based on a Phosphoramidite Amine-Exchange Reaction;The Journal of Organic Chemistry;1997-10-01
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