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Honda et al., 2003 - Google Patents
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Honda et al., 2003 - Google Patents

A Formal Total Synthesis of Securinine via an Intramolecular (4+ 2) Cycloaddition Reaction

Honda et al., 2003

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Document ID
13233206519954041608
Author
Honda T
Namiki H
Kudoh M
Nagase H
Mizutani H
Publication year
Publication venue
Heterocycles-Sendai Institute of Heterocyclic Chemistry

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An intramolecular Diels-Alder reaction of the enol ester derived from 2-acetylpyridine and sorbic anhydride gave the cycloaddition product, stereoselectively, which was further converted into the key intermediate for the synthesis of securinine. Securinine, 1 a member …
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    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
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