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- W2949460110 abstract "Lithium 1-alkoxyeneselenolates 2 in tetrahydrofuran were characterized by 1H NMR for the first time. Their reaction with propargyl bromide was found to proceed through a propargylic rearrangement to generate allenic selenoic acid O-esters 3, which led to poly-substituted selenophenes in moderate yields under reflux." @default.
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- W2949460110 date "1995-04-01" @default.
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- W2949460110 title "Reaction of lithium 1-alkoxyeneselenolates with propargylic bromides: One-pot conversion to poly-substituted selenophenes" @default.
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- W2949460110 doi "https://doi.org/10.1016/0040-4039(95)00402-x" @default.
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