CAS#112793-01-8 | N6-(2-Deoxy-

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

‐diisopropylamino)phosphinyl‐2′‐deoxycytidine N6 ‐Benzoyl‐5′‐O ‐(4,4′‐dimethoxytrityl)‐3′‐O ‐bis(N ,N ‐diisopropylamino)phosphinyl‐2′‐deoxyadenosine

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

Figure 4.52.1 Synthesis of 2′‐ O ‐(aminooxymethyl)ribonucleosides (S.5 a‐d ). Abbreviations: BP , a uracil‐1‐yl, b N 4 ‐benzoylctytosin‐1‐yl, c N 6 ‐isobutyryladenin‐9‐yl, d N 2 ‐phenoxyacetylguanin‐9‐yl; DBU, 1,8‐diazabicyclo[5.4.0]undec‐7‐ene; B

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

analogue synthesis. J. Org. Chem. 66:8592‐8598.    Wan, Z.‐K., Binnun, E., Wilson, D.P., and Lee, J. 2005. A highly facile and efficient one‐step synthesis of N6‐adenosine and N6‐2′