Applications of green chemistry in the manufacture of oligonucleotide drugs (original) (raw)

UnyLinker: An Efficient and Scaleable Synthesis of Oligonucleotides Utilizing a Universal Linker Molecule: A Novel Approach To Enhance the Purity of Drugs

LUCIO MENDEZ

Organic Process Research & Development, 2008

View PDFchevron_right

Green approaches for the synthesis of nucleotides, their conjugates and analogues

Béatrice Roy

Phosphorus Sulfur and Silicon and The Related Elements, 2020

View PDFchevron_right

Efficient synthesis of antisense phosphorothioate oligonucleotides using a universal solid support

Andrei Guzaev, Vasulinga Ravikumar

Tetrahedron, 2006

View PDFchevron_right

Solid-phase synthesis of 5′-triantennary N-acetylgalactosamine conjugated antisense oligonucleotides using phosphoramidite chemistry

Thazha Prakash

Bioorganic & Medicinal Chemistry Letters, 2015

View PDFchevron_right

Phosphoramidites and solid supports based on N-substituted 2,4-dihydroxybutyramides: universal reagents for synthesis of modified oligonucleotides

Dmitry Stetsenko

Tetrahedron, 2006

View PDFchevron_right

Control of phosphorothioate stereochemistry substantially increases the efficacy of antisense oligonucleotides

david butler

Nature biotechnology, 2017

View PDFchevron_right

Solid-Phase Synthesis of Modified Oligonucleotides

Ramon Eritja

International Journal of Peptide Research and Therapeutics, 2006

View PDFchevron_right

Liquid‐Phase Oligonucleotide Synthesis: Past, Present, and Future Predictions

Yogesh Sanghvi

Current protocols in nucleic acid chemistry, 2019

View PDFchevron_right

Modified oligonucleotides: IV solid phase synthesis and preliminary evaluation of phosphorothioate RNA as potential antisense agents

Francois Morvan

Tetrahedron Letters, 1990

View PDFchevron_right

Phosphoramidite reagents and solid-phase supports based on hydroxyprolinol for the synthesis of modified oligonucleotides

Sergey Gontarev

Russian Journal of Bioorganic Chemistry, 2017

View PDFchevron_right

An improved synthesis of oligodeoxynucleotide N34∀P54 phosphoramidates and their chimera using hindered phosphoramidite monomers and a novel handle for reverse phase purification

Mark Nguyen

2000

View PDFchevron_right

Large-scale synthesis of high purity “Phos reagent” useful for oligonucleotide therapeutics

Yogesh Sanghvi

Journal of Organometallic Chemistry, 2005

View PDFchevron_right

The pro-oligonucleotide approach: solid phase synthesis and preliminary evaluation of model pro-dodecathymidylates

Francois Morvan

Nucleic Acids Research, 1998

View PDFchevron_right

Prevention of guanine modification and chain cleavage during the solid phase synthesis of oligonucleotides using phosphoramidite derivatives

Nassim Usman

Nucleic Acids Research, 1986

View PDFchevron_right

Synthesis, biophysical properties and biological activity of second generation antisense oligonucleotides containing chiral phosphorothioate linkages

sam lee

Nucleic Acids Research, 2014

View PDFchevron_right

Solid-phase synthesis of base-sensitive oligonucleotides

Pasi Virta

Arkivoc, 2008

View PDFchevron_right

Oligonucleotides: Current Trends and Innovative Applications in the Synthesis, Characterization, and Purification

Massimo Morbidelli

Biotechnology Journal, 2020

View PDFchevron_right

Antisense Oligonucleotides Containing Conformationally Constrained 2′,4′-( N Methoxy)aminomethylene and 2′,4′-Aminooxymethylene and 2′- O ,4′- C -Aminomethylene Bridged Nucleoside Analogues Show Improved Potency in Animal Models

Chris Black

Journal of Medicinal Chemistry, 2010

View PDFchevron_right

Convergent Solution Phase Synthesis of Chimeric Oligonucleotides by a 2+2 and 3+3 Phosphoramidite Strategy

Kaushik Chanda

Australian Journal of Chemistry, 2010

View PDFchevron_right

Mixed-Backbone oligonucleotides as second-generation antisense agents with reduced phosphorothioate-related side effects

Carl Saxinger

Bioorganic & Medicinal Chemistry Letters, 1998

View PDFchevron_right

Synthesis of branched antisense oligonucleotides having multiple specificities

Marvin Rubenstein

Medical Hypotheses, 2006

View PDFchevron_right

An improved synthesis of oligodeoxynucleotide N3'->P5' phosphoramidates and their chimera using hindered phosphoramidite monomers and a novel handle for reverse phase purification

Larry DeDionisio

Nucleic Acids Research, 1998

View PDFchevron_right

Mesyl phosphoramidate antisense oligonucleotides as an alternative to phosphorothioates with improved biochemical and biological properties

Valentin Vlasov

Proceedings of the National Academy of Sciences of the United States of America, 2019

View PDFchevron_right

3′-3′-linked oligonucleotides: Synthesis and stability studies

Carole Chaix

Bioorganic & Medicinal Chemistry Letters, 1996

View PDFchevron_right

The Dimethoxytrityl Resin Product Anchored Sequential Synthesis Method (DMT PASS): A Conceptually Novel Approach to Oligonucleotide Synthesis

David Sebesta

Organic Process Research & Development, 2000

View PDFchevron_right

Antisense oligodeoxynucleotides: synthesis, biophysical and biological evaluation of oligodeoxynucleotides containing modified pyrimidines

Yogesh Sanghvi

Nucleic Acids Research, 1993

View PDFchevron_right

Antisense Oligonucleotides: An Emerging Area in Drug Discovery and Development

Karishma Dhuri

Journal of Clinical Medicine

View PDFchevron_right

Novel chemoenzymatic protocol for the synthesis of 3′-O- dimethoxytrityl-2′-deoxynucleoside derivatives as building blocks for oligonucleotide synthesis

Yogesh Sanghvi

2006

View PDFchevron_right

Intermolecular radical CC bond formation: Synthesis of a novel dinucleoside linker for non-anionic antisense oligonucleosides

Dan Cook

Tetrahedron Letters, 1992

View PDFchevron_right

Optimized Automated Solid Phase Synthesis of Oligonucleotides and Derivatives

Gerald Grübler

Zeitschrift für Naturforschung B, 1998

View PDFchevron_right

A new solid-phase synthesis of oligonucleotides 3′-conjugated with peptides

Enrico Bucci

Bioorganic & Medicinal Chemistry, 1999

View PDFchevron_right

Synthesis of 5′-GalNAc-Conjugated Oligonucleotides: A Comparison of Solid and Solution-Phase Conjugation Strategies

Andrew Rodriguez

Molecules, 2017

View PDFchevron_right