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2000
Volume 11, Issue 3
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

The synthesis of (+/-)-neuchromenin, a known natural product that induces neurite outgrowth of PC12 cells, is described. The total synthesis involved constructing a chromone ring from sesamol and coupling this intermediate to an aldehyde by a Morita-Baylis-Hillman reaction (MBH). The MBH adduct was cyclized under acidic conditions followed by removal of a methylene group to afford (+/-)-neuchromenin in 9 steps from sesamol.

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/content/journals/loc/10.2174/15701786113106660088
2014-03-01
2025-10-05
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/content/journals/loc/10.2174/15701786113106660088
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  • Article Type:
    Research Article
Keyword(s): Baylis-Hillman Reaction; fries rearrangement; Neuchromenin; sesamol
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