Synthesis of Antibiotic Stilbenes by Reductive Metalation of 3,4,5-Trimethoxybenzaldehyde Dimethyl Acetal

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dc.contributor.authorUgo Azzena
dc.contributor.authorMaria Vittoria Idini
dc.contributor.authorLuciano Pilo
dc.date.accessioned2012-11-09T07:11:00Z
dc.date.accessioned2025-02-17T13:59:31Z
dc.date.available2012-11-09T07:11:00Z
dc.date.issued2012-11-08
dc.descriptionReductive metalation of 3,4,5-trimethoxybenzaldehyde dimethyl acetal followed by reaction with suitable electrophiles is the key step of a reaction sequence leading to the synthesis of naturally occurring 4-alkyl-3,5-dihydroxy-substituted trans-stilbenes having antibiotic activity.en_US
dc.description.abstractReductive metalation of 3,4,5-trimethoxybenzaldehyde dimethyl acetal followed by reaction with suitable electrophiles is the key step of a reaction sequence leading to the synthesis of naturally occurring 4-alkyl-3,5-dihydroxy-substituted trans-stilbenes having antibiotic activity.en_US
dc.identifier.urihttps://dl.ftveti.edu.et/handle/123456789/3957
dc.language.isoenen_US
dc.subjectSynthesis of Antibiotic Stilbenes by Reductive Metalation of 3,4,5-Trimethoxybenzaldehyde Dimethyl Acetalen_US
dc.titleSynthesis of Antibiotic Stilbenes by Reductive Metalation of 3,4,5-Trimethoxybenzaldehyde Dimethyl Acetalen_US
dc.typeArticleen_US

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