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- W2462603149 abstract "A selenium-mediated strategy for the stereoselective synthesis of substituted tetrahydropyrans and isochromans has been developed starting from δ-phenylseleno ketones. After enantioselective reduction, the chiral nonracemic phenylseleno alcohols were oxidized to the corresponding selenones, which underwent an effcient 6-exo-tet ring-closure reaction." @default.
- W2462603149 created "2016-07-22" @default.
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- W2462603149 date "2015-08-11" @default.
- W2462603149 modified "2023-09-23" @default.
- W2462603149 title "Stereoselective Synthesis of Substituted Tetrahydropyrans and Isochromans by Cyclization of Phenylseleno Alcohols" @default.
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- W2462603149 doi "https://doi.org/10.1021/acs.joc.5b01199" @default.
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