(5-Fluoro-1H-indol-3-yl)-2-met

Biotinylation of a Propargylated Cyclic (3′‐5′) Diguanylic Acid and of Its Mono‐6‐Thioated Analog Under “Click” Conditions

Yan, H. and López Aguilar, A. 2007. Synthesis of 3′,5′‐cyclic diguanylic acid (cdiGMP) using 1‐(4‐chlorophenyl)‐4‐ethoxypiperidin‐4‐yl as a protecting group for 2′‐hydroxy functions of ribonucleosides. Nucleosides Nucleotides Nucleic Acids 26:189‐204

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

triethylammonium acetate pH 7.0, a linear gradient of 1% MeCN/min is pumped at a flow rate of 1 mL/min for 40 min. Abbreviation: Ura, uracil‐1‐yl. Adapted from Cieślak et al. () by permission of Oxford University Press