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The Total Synthesis of Retrojusticidin B, Justicidin E, and Helioxanthin
Tzu-Ting Kao1,2, Chun-Cheng Lin1, Kak-Shan Shia2
1†Department of Chemistry, National Tsing Hua University, Hsinchu 30013, Taiwan, R.O.C.
Abstract:
Making use of a tandem free radical cyclization process mediated by Mn(OAc)3 as a key operation, the total synthesis of retrojusticidin B, justicidin E, and helioxanthin has been concisely achieved in four or five steps in an overall yield of 45, 33 and 44%, respectively, from a common starting material 5.
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