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Adenosine, N-benzoyl-2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]-, 3'-(2,2,2-trifluoroethyl trimethylsilyl phosphite)

Base Information
  • Chemical Name:Adenosine, N-benzoyl-2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]-, 3'-(2,2,2-trifluoroethyl trimethylsilyl phosphite)
  • CAS No.:114071-79-3
  • Molecular Formula:C28H41F3N5O6PSi2
  • Molecular Weight:687.803
  • Hs Code.:
  • Mol file:114071-79-3.mol
Adenosine, N-benzoyl-2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]-,
3'-(2,2,2-trifluoroethyl trimethylsilyl phosphite)

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Chemical Property of Adenosine, N-benzoyl-2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]-, 3'-(2,2,2-trifluoroethyl trimethylsilyl phosphite)
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Technology Process of Adenosine, N-benzoyl-2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]-, 3'-(2,2,2-trifluoroethyl trimethylsilyl phosphite)

There total 1 articles about Adenosine, N-benzoyl-2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]-, 3'-(2,2,2-trifluoroethyl trimethylsilyl phosphite) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 2 steps
1: sulfuryl chloride / CH2Cl2 / 1.) 0 deg C, 2.) 30 min, room temperature
2: triethylamine / CH2Cl2 / 1 h
With sulfuryl dichloride; triethylamine; In dichloromethane;
DOI:10.1016/S0040-4039(00)95534-5
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