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- W1969970385 abstract "The construction of the hetisane group of alkaloids, of which the extensively bridged nominine 17 is the simplest member, poses the ultimate challenge for those interested in the synthesis of the C20 diterpene alkaloids. We describe the synthesis of an advanced intermediate toward this goal. The key steps include reductive acylation, reductive deoxygenation, Birch reduction, and an intramolecular Lewis acid-catalyzed 1,6-addition of a carbamate to a dienone." @default.
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- W1969970385 date "2007-11-21" @default.
- W1969970385 modified "2023-09-23" @default.
- W1969970385 title "Studies toward the Total Synthesis of Nominine" @default.
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- W1969970385 doi "https://doi.org/10.1021/jo701995u" @default.
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