Graduate School of Pharmaceutical Sciences, University of Tokyo
Graduate School of Pharmaceutical Sciences, Nagoya University
Graduate School of Pharmaceutical Sciences, Tohoku University
2016 Volume 64 Issue 7 Pages 800-804
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Conversion of readily available vindoline to 11-mesyloxytabersonine, a versatile synthetic intermediate for indole alkaloids, has been achieved by a 9-step sequence in 39% overall yield.
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