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- W2013647585 abstract "The synthesis of two rotationally restricted phenolic analogs (1a and 1b) of the neurotransmitter serotonin have been accomplished. The syntheses of 8.9-dihydropyrano[3,2-e]indole (13a) and 7,8-dihydropyrano[2,3-f]indole (13b), which formed the template for these targets, are outlined. These novel fused-indoles represent rotationally restricted phenolic analogs of 5-hydroxyindole. The reaction sequence of Claisen rearrangement, olefin hydroxylation, and intramolecular Mitsunobu reaction was used to form the fused-dihydropyran rings." @default.
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- W2013647585 date "1992-01-01" @default.
- W2013647585 modified "2023-10-16" @default.
- W2013647585 title "The synthesis of pyrano[3,2-e]indoles and pryano[2,3-f]indoles as rotationally restricted phenolic analogs of the neurotransmitter serotonin" @default.
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- W2013647585 doi "https://doi.org/10.1016/s0040-4020(01)88200-4" @default.
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