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- W977376722 abstract "The regiospecific reduction and Favorskii rearrangement of enantiopure tetrabromoepifenchone, which could be easily obtained by bromination of camphor, have been investigated. The selective formation of new functionalized chiral bicyclo[2.2.1]heptane and bicyclo[2.1.1]hexane derivatives in good yield has been demonstrated. Our approach provides a simple pathway for the large-scale synthesis of a wide range of novel functionalized bicyclic terpenoids starting from easily available camphor." @default.
- W977376722 created "2016-06-24" @default.
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- W977376722 date "2015-08-01" @default.
- W977376722 modified "2023-09-27" @default.
- W977376722 title "Tetrabromoepifenchone: a convenient precursor for the synthesis of chiral bicyclo[2.2.1]heptane and bicyclo[2.1.1]hexane derivatives" @default.
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- W977376722 doi "https://doi.org/10.1016/j.tetasy.2015.06.012" @default.
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