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- W2109609192 abstract "This communication describes the preparation and behavior of ether-substituted 1-boronobutadienes 1 and 2 in the Vaultier tandem [4+2]/allylboration three-component reaction involving electron-poor dienophiles and aldehydes. Whereas diene 1 failed to undergo the second, allylboration step of this process, diene 2 reacted with maleimides to give products 12, and even reacted with moderately activated dienophiles such as acrylates and acrylamide derivative 14 to provide a new stereoselective approach to the synthesis of hydroxyalkylated cyclohexene derivatives." @default.
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- W2109609192 date "2003-03-01" @default.
- W2109609192 modified "2023-10-09" @default.
- W2109609192 title "New electronically enriched boronobutadienes for the synthesis of hydroxylated cyclohexenes via tandem [4+2]/allylboration" @default.
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- W2109609192 doi "https://doi.org/10.1016/s0040-4039(03)00164-3" @default.
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