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- W2015512145 abstract "Base-catalysed isomerization of trans-3-methoxy-1-phenylpropene (A) yields stereospecifically as the initial product cis-1-methoxy-3-phenylpropene (B). This is caused by the (intermediate) formation of the cis-1-methoxy-trans-3-phenylallyl anion (II-1), which is energetically favoured over the trans-isomeric anion (I). The NMR spectra of I and II-1 are described." @default.
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- W2015512145 date "2010-09-02" @default.
- W2015512145 modified "2023-10-09" @default.
- W2015512145 title "Stereochemistry of base-catalysed double-bond migration in allyl ethers" @default.
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- W2015512145 doi "https://doi.org/10.1002/recl.19700890106" @default.
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