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- W2950920847 abstract "In chlorination, bromination, iodination, nitration, sulfonation, formylation, and trifluoroacetylation of [1]benzothieno[3,2- b ]furan ( 1 ) the substituent enters the 2-position. The said halogenations go by the addition-elimination mechanism. When the substitution is continued, the second substituent enters the 6-position of heterocycle 1 . The 1 H and 13 C NMR spectra have been completely assigned. Substituent effects on NMR parameters are discussed." @default.
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- W2950920847 date "1996-01-01" @default.
- W2950920847 modified "2023-10-06" @default.
- W2950920847 title "Electrophilic Substitution Reactions of [1]Benzothieno[3,2-b]furan" @default.
- W2950920847 doi "https://doi.org/10.1135/cccc19960888" @default.
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