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Assembly of a Key Dienic Intermediate for Tetrodotoxin via a Machetti–DeSarlo Reaction

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Figshare2016-02-18 更新2026-04-29 收录
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A route to a racemic diene intermediate for the synthesis of tetrodotoxin is described. Key steps of the sequence leading to such a compound include the oxidative amidation of a phenol, a Cu­(II)-catalyzed cyclocondensation of a nitroketone with an olefin (Machetti–DeSarlo reaction), and a nucleophilic fragmentation of the resulting isoxazoline. Several unusual reactions encountered in the course of this study are thoroughly discussed.

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2016-02-18
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