Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. The appropriate choice can avoid electrode passivation, which strongly inhibit the efficient activation of substrates. 20419-68-5, Name is 2,6-Dichloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine, molecular formula is C10H10Cl2N4O. In a Article，once mentioned of 20419-68-5, Recommanded Product: 20419-68-5
A metal free approach was developed for accessing 4-aryl chromans and 1-aryl tetralins from their commercially available building blocks. This operationally simple protocol was well tolerated with the presence of labile functional groups, providing biologically relevant chemical libraries, which can be used for late stage modification. Dearylated analogues of the drugs Ormeloxifene and Lasofoxifene were synthesized using this approach.
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Reference：
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics