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- W2022371427 startingPage "1041" @default.
- W2022371427 abstract "Lewis acid-catalysed alkylation of para-substituted phenols using α-chloro sulphides as electrophiles yields sulphenylated γ-lactones which can be desulphurised with zinc in acetic acid or Raney nickel. This synthesis has been applied to p-cresol, 2-naphthol, and two phenolic dihydrocinnamates. Alkylation of 1,4-dimethoxybenzene yields homogentisic acid dimethyl ether after desulphurisation and hydrolysis." @default.
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- W2022371427 date "1990-01-01" @default.
- W2022371427 modified "2023-09-27" @default.
- W2022371427 title "Organic synthesis with α-chloro sulphides. Preparation of aromatic γ-lactones from phenols and α-chloro sulphide carboxylates" @default.
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- W2022371427 doi "https://doi.org/10.1039/p19900001041" @default.
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