85817-34-1;1-苯基-3-羟甲基哌嗪 , -;(4

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

  Figure 1.26.3 Two possible modes by which the C‐6 amide could react with BOP leading to O 6 ‐(benzotriazol‐1‐yl)inosine derivatives. View Image

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

  Figure 4.52.2 Preparation of 5′‐ O ‐aminooxymethyl‐2′‐deoxythymidine (S.10 ). Abbreviations: Lev, levulinyl; Thy, thymin‐1‐yl; DBU, 1,8‐diazabicyclo[5.4.0]undec‐7‐ene. Adapted from Cieślak et al

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

‐(1‐(2‐((2‐Azidoethyl)(2‐(bis(4‐methoxyphenyl)(phenyl)methoxy)ethyl)amino)‐2‐oxoethyl)‐N 4 ‐(benzoyl)cytosin‐1‐yl) (19 ; Basic Protocol 3) Tetrahydrofuran (THF), anhydrous, ≥99.9% pure