2′-脱氧鸟苷-5′-单磷酸二钠盐;33430-61-4;H

Uridine 2′‐Carbamates: Facile Tools for Oligonucleotide 2′‐Functionalization

7.0 (DMTr‐ON, HPLC) Mobile phase B: 100% CH 3 CN (DMTr‐ON, HPLC) 1 to 400 mM sodium perchlorate in 20 mM Tris·Cl (pH

Synthesis of Triazole‐Nucleoside Phosphoramidites and Their Use in Solid‐Phase Oligonucleotide Synthesis

5 ) 2′‐TBDMS guanosine (n ‐ibu) phosphoramidite, ≥98% pure (ChemGenes, cat. no. ANP‐5673) 2′‐TBDMS cytidine (n ‐bz) phosphoramidite, 97.4% pure (ChemGenes

Synthesis and Application of Highly Reactive Amino Linkers for Functional Oligonucleotides

  Figure 4.48.5 HPLC analyses of (A ) The ssH‐modified ONT and (B ) The C6‐modified ONT before and after open column purification. The ONT sequences are 5′‐X‐TCTTCCAAGCAATTCCAATGAAAGC (X‐25, X = ssH and C6