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- W2949250337 abstract "The first total syntheses of new monoterpene alkaloids (-)-incarvilline, (+)-incarvine C, and (-)-incarvillateine, corresponding to the natural enantiomers, have been accomplished. The strategy for the synthesis of these natural products utilized 6-epi-incarvilline as a common precursor, which was assembled by a three-component coupling reaction using (4S)-4-siloxy-2-cyclopenten-1-one to construct an appropriately trisubstituted cyclopentanone, followed by ring closure to the cis-perhydro-2-pyrindine skeleton by means of a reductive Heck-type reaction. An alternative ring closure to the cis-perhydro-2-pyrindine skeleton was also carried out employing intramolecular enone-olefin [2+2] photocycloaddition. Furthermore, topochemically controlled [2+2] photodimerization of ferulic acid derivatives in the solid state for the stereospecific construction of a 1,2,3,4-tetrasubstituted cyclobutane ring was investigated as a means to access (-)-incarvillateine." @default.
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- W2949250337 date "2009-01-01" @default.
- W2949250337 modified "2023-10-16" @default.
- W2949250337 title "Total Synthesis of Incarvillateine and Related Alkaloids" @default.
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- W2949250337 doi "https://doi.org/10.5059/yukigoseikyokaishi.67.369" @default.
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