2-(6-Bromo-1H-benzimidazol-2-y

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

Release of DNA Oligonucleotides and Their Conjugates from Controlled‐Pore Glass Under Thermolytic Conditions

oligonucleotides conjugated with exemplary reporter or functional groups, either at the 3??terminus or at both 3?? and 5??termini, is also described. Curr. Protoc. Nucleic Acid Chem. 35:3.17.1?3.17.21. © 2008 by John Wiley & Sons, Inc. Keywords