1984
DOI: 10.1016/s0040-4039(01)80152-0
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A facile Pd(II)-mediated synthesis of bicyclo[3.3.1]nonadienones

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1984
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Cited by 25 publications
(3 citation statements)
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“…The ring closure is regarded as proceeding by nucleophilic attack of the enol ether double bond on Pd(II)-complexed exocyclic olefin. 29 This synthesis started with the Birch reduction of substituted benzoic acid followed by allylation of the resulting cyclohexadiene acid dianion.…”
Section: Scheme 18mentioning
confidence: 99%
“…The ring closure is regarded as proceeding by nucleophilic attack of the enol ether double bond on Pd(II)-complexed exocyclic olefin. 29 This synthesis started with the Birch reduction of substituted benzoic acid followed by allylation of the resulting cyclohexadiene acid dianion.…”
Section: Scheme 18mentioning
confidence: 99%
“…The total synthesis of selagine (I), a Lycopodium alkaloid whose structure was determined over twenty years ago by Wiesner, Valenta, and co-workers (I), still remains an open challenge in the literature and recent publications which have appeared (2)(3)(4)(5) attest to the interesting problems of regiochemistry posed by this molecule.…”
mentioning
confidence: 99%
“…3.1]nonadienones92 and to a total synthesis of quadrone. 93 as stoichiometric oxidant in acetic acid leads to an oxidative cyclization reaction (eqs 46 and 47).…”
mentioning
confidence: 99%