Jaehoon Bae

Synthesis of N-(2-methylpropyl)-2E-undecene-8,10-diynamide, a novel constituent of Echinacea angustifolia

The first synthesis of a diacetylenic amide from Echinacea is reported. The key steps included the reaction of an aldehyde with the monoanion of a diacetylene and the reductive removal of a propargylic alcohol.

Synthesis and natural distribution of anti-inflammatory alkamides from Echinacea.

The synthesis of the alkamides 2Z,4E-undeca-2,4-dien-8,10-diynoic acid isobutyl amide (1) and 2Z,4E-undeca-2,4-dien-8,10-diynoic acid isobutyl amide (5) was accomplished by organometallic coupling followed by introduction of the doubly unsaturated amide moiety. The distribution of these two amides in accessions of the nine species of Echinacea was determined.

The Synthesis and Natural Distribution of the Major Ketone Constituents in Echinacea pallida

The first synthesis of a series of ketones naturally occurring in E. pallida is described. The natural distribution of these ketones among different Echinacea species is also reported.

Phytochemicals from Echinacea and Hypericum: A Direct Synthesis of Isoligularone

Abstract Reaction of trienes with α,β‐unsaturated aldehydes produces bicyclic products via a tandem Diels–Alder/ene reaction. The adduct from tiglic aldehyde was converted into isoligularone by conversion to a furan followed by benzylic oxidation.