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- W2012129863 abstract "The first stereoselective synthesis of epimeloscine has been accomplished in 13 total steps with a longest linear sequence of 10 steps. The core of the synthesis takes only five steps, the key ones being acylation, stereoselective tandem radical cyclization of a divinylcyclopropane to make two rings, and group-selective ring-closing metathesis of the resulting divinylcyclopentane to make the last ring." @default.
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- W2012129863 date "2011-06-16" @default.
- W2012129863 modified "2023-09-30" @default.
- W2012129863 title "A Short Total Synthesis of (±)-Epimeloscine and (±)-Meloscine Enabled by a Cascade Radical Annulation of a Divinylcyclopropane" @default.
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- W2012129863 doi "https://doi.org/10.1021/ja2042854" @default.
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