The synthetic routes utilized for the preparation of the prerequisite alkyl
Stereoselective construction of the azabicyclic core applicable to the biologically important polyguanidinium alkaloids batzelladine A and D using a free radical cyclization
Scheme 1
Scheme 1 summarizes the synthetic routes utilized for the preparation of the prerequisite alkyl bromides 6a/c and acyl selenides 6b/d for our initial study. Treatment of the secondary alcohol 4 with 3-N-benzoyl-protected uracil and thymine 3a/b under Mitsunobu conditions furnished 5a and 5b in 81% and 72% yield, respectively.
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