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Heck Transformations of Biological Compounds Catalyzed by Phosphine-Free Palladium.

ABSTRACT: The development and optimization of synthetic methods leading to functionalized biologically active compounds is described. Two alternative pathways based on Heck-type reactions, employing iodobenzene or phenylboronic acid, were elaborated for the arylation of eugenol and estragole. Cinnamyl alcohol was efficiently transformed to saturated arylated aldehydes in reaction with iodobenzene using the tandem arylation/isomerization sequential process. The arylation of cinnamyl alcohol with phenylboronic acid mainly gave unsaturated alcohol, while the yield of saturated aldehyde was much lower. Catalytic reactions were carried out using simple, phosphine-free palladium precursors and water as a cosolvent, following green chemistry rules as much as possible.

SUBMITTER: Tarnowicz-Ligus S

PROVIDER: S-EPMC6225119 | biostudies-literature | 2018 Sep

REPOSITORIES: biostudies-literature

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Heck Transformations of Biological Compounds Catalyzed by Phosphine-Free Palladium.

Tarnowicz-Ligus Stanisława S Trzeciak Anna M AM

Molecules (Basel, Switzerland) 20180901 9

The development and optimization of synthetic methods leading to functionalized biologically active compounds is described. Two alternative pathways based on Heck-type reactions, employing iodobenzene or phenylboronic acid, were elaborated for the arylation of eugenol and estragole. Cinnamyl alcohol was efficiently transformed to saturated arylated aldehydes in reaction with iodobenzene using the tandem arylation/isomerization sequential process. The arylation of cinnamyl alcohol with phenylboro ...[more]

PMID: 30200476

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