{1-[2-(Dimethylamino)ethyl]pyr

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

Uracil‐1‐yl acetic acid (2 ; protocol 1 ) N ‐(2‐((tert ‐Butyldimethylsilyl)oxy)ethyl)prop‐2‐yn‐1‐amine (8 ; protocol

Two‐Step, One‐Pot Synthesis of Inosine, Guanosine, and 2′‐Deoxyguanosine O6‐Ethers via Intermediate O6‐(Benzotriazol‐1‐yl) Derivatives

for the etherification at the O 6 ?position of silyl?protected inosine, guanosine, and 2??deoxyguanosine is described. Typically, a THF solution of the silylated nucleoside is treated with 1H ?benzotriazol?1?yloxy?tris(dimethylamino)phosphonium hexafluorophosphate (BOP

Convenient and Efficient Approach to the Permanent or Reversible Conjugation of RNA and DNA Sequences with Functional Groups

with an analytical sample of N ‐(4‐cyanobut‐1‐yl)‐5‐(dimethylamino)naphthalene‐1‐sulfonamide. Conditions: RP‐HPLC analysis is performed under conditions identical to those described for the fluoride‐assisted conversion of S.11 a to uridine in Figure . Abbreviation